Tunicamycin analogues

ABSTRACT

The invention relates to tunicamycin analogues which are compounds according to Formula (I), or pharmaceutically acceptable salts thereof, (I) Wherein [Base] and R 1  to R 9  are as defined herein. The tunicamycin analogues are useful in the prevention or treatment of bacterial infection, in particular of tuberculosis.

FIELD OF THE INVENTION

The present invention relates to a series of lipid-altered tunicamycin analogues which are useful as antibacterial agents. The invention also relates to the use of lipid-altered tunicamycin analogues as antibacterial agents and to the provision of pharmaceutical compositions comprising lipid-altered tunicamycins.

BACKGROUND

Antibiotics with broad activity yet unique modes of action are desirable for tackling pathogenic infections. However, the current range of effective antibiotics is shrinking as pathogens acquire immunity towards commonly prescribed antibiotics. There is therefore a need to provide new antibiotics with broad activity against pathogens.

Tunicamycin is a widely known and naturally occurring nucleoside antibiotic that has been demonstrated to exhibit antibacterial activity. The antibacterial properties of tunicamycin derive from the transfer of a bacterially unique sugar-1-phosphoryl unit onto a bacteria specific lipid, catalysed by the transmembrane enzyme MraY translocase. MraY catalyses the formation of the key peptidoglycan precursor undecaprenyl-pyrophosphoryl-N-acetylmuramoyl pentapeptide, a key peptidoglycan precursor. MraY exists in both gram-positive and gram-negative bacteria. However, there are currently no clinically approved antibiotics which target MraY.

Although tunicamycin is a potent, naturally-occurring nucleoside antibiotic, it is also highly toxic towards eukaryotic cells. For this reason, the clinical use of tunicamycin in the treatment of or prophylaxis against bacterial infection is not feasible. The toxicity of tunicamycin arises from its ability to inhibit both N-glycosylation and N-acylation of eukaryotic proteins. For instance, it is believed that specific binding to the active site of UDP-GlcNAc:dolichyl phosphate GlcNAc-1-phosphate transferase (GTP) blocks production of the lipid-linked precursor dolichyl-pyrophosphory-N-acetyl-glucosamine (Dol-PP-GlcNAc) and terminates asparagine-linked glycoprotein synthesis at the first committed step. This property has, however, made tunicamycin a valuable biochemical tool in glycobiology to study post-translational modification of eukaryotic proteins.

Tunicamycin as a natural product is a mixture of homologous secondary metabolites (see structure below), produced by several Streptomyces species, and belongs to the same family of nucleoside secondary metabolites as streptovirudin and corynetoxin. The components within the naturally occurring tunicamycin mixture differ in the length of the lipid chains on the tunicamine core, but the separation of these homologues is a difficult and tedious process. Early studies revealed that factors including the length of the lipid chain on the tunicamine core, the degree of saturation and the particular isomer all interplayed in determining the bioactivity of the relevant homologue in prokaryotes and eukaryotes. As different homologues cannot be easily isolated, almost all studies in the literature use tunicamycin as a mixture.

Natural Tunicamycin:

SUMMARY OF THE INVENTION

The inventors have surprisingly found that it is possible to create analogues of tunicamycin in which the antibacterial activity is separated from the mammalian toxicity. In particular, the inventors have found that by modifying the sugar attached to the tunicamine core to incorporate a lipid, ‘lipid-altered’ tunicamycin analogues displaying enhanced potency against pathogenic and non-pathogenic bacteria, yet minimal cytotoxicity towards mammalian cells, can be obtained.

Accordingly, the invention provides an oligosaccharide which is a compound according to Formula (I), or a pharmaceutically acceptable salt thereof,

wherein:

-   -   [Base] is a natural nucleobase selected from adenine, cytosine,         guanine, thymine and uracil;     -   each R¹, which may be the same or different, is independently H,         OH, —OPO(OH)₂, or halogen;     -   each R², which may be the same or different, is independently H,         halogen, or C₁ to C₂ alkyl;     -   R³ and R⁴, which may be the same or different, are each         independently H, OH, halogen, C₁ to C₂ alkyl, C₁ to C₂ alkoxy,         or —NR¹⁰R¹¹;     -   each R⁵, which may be the same or different, is independently H,         halogen, or C₁ to C₂ alkyl;     -   each R⁶, which may be the same or different, is independently         OH, halogen, —OPO(OH)₂, —OCO₂CH₃, —NHCOCH₃ or C₁ to C₂ alkoxy;     -   one or more R⁷ and/or one or more R⁸ is a group —NHC(O)R⁹; the         remaining groups R⁷, which may be the same or different, are         independently H, halogen, or C₁ to C₂ alkyl; and the remaining         groups R⁸, which may be the same or different, are independently         OH, halogen, —OPO(OH)₂, or —OCO₂CH₃, —NHCOCH₃ or C₁ to C₂         alkoxy;     -   each R⁹, which may be the same or different, is independently C₃         to C₂₀ alkyl, C₃ to C₂₀ alkenyl, or C₃ to C₂₀ alkynyl, wherein         R⁹ may be unsubstituted or may be substituted by from 1 to 6         substituents selected from halogen, OH, C₁ to C₄ alkoxy and         —NR¹⁰R¹¹; and     -   each R¹⁰ and R¹¹, which may be the same or different, is         independently H or C₁ to C₄ alkyl.

The invention also provides a pharmaceutical composition comprising an oligosaccharide as described herein, and a pharmaceutically acceptable carrier or diluent.

The invention also provides an oligosaccharide as described herein, or a pharmaceutical composition as described herein, for use in treating or preventing bacterial infection in a subject.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 shows results of the Kirby-Bauer disc diffusion susceptibility test conducted using Bacillus subtilis and Bacillus cereus as test organisms using compounds according to the invention and natural tunicamycin.

FIG. 2 shows corresponding results for the organism Pseudomonas aeruginosa.

FIG. 3 shows dose response curves from HepG2 and HEK293 cell proliferation tests for TM.

FIG. 4 shows the results of cell morphology tests, including cell images of HEK293 cells in the presence of TM and two compounds of the invention over two fold dilutions.

FIG. 5 shows a pharmacokinetic curve for di-N-octanoyl-tunicamycin (also referred to as compound E3 or TM-8) after intraperitoneal injection in sixteen mice. The initial dose was 30 mg/kg. The x-axis indicates the time in hours after the initial injection and the y-axis indicates the blood plasma concentration of TM-8 in μg/mL in the mice.

FIG. 6 shows time-of-flight mass spectra (TOF-MS) for tunicamycin obtained from two different sources. FIG. 6(a) contains the TOF-MS for crude tunicamycin extracted from an S. chartreusis NRRL 3882 culture, while FIG. 6(b) contains the TOF-MS for a commercial tunicamycin standard obtained from Sigma Aldrich.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, a C₃ to C₂₀ alkyl group is a linear or branched alkyl group containing from 3 to 20 carbon atoms. Typically a C₃ to C₂₀ alkyl group is a C₄ to C₁₆ alkyl group, e.g. a C₆ to C₁₂ alkyl group. A C₆ to C₁₂ alkyl group is a linear or branched alkyl group containing from 6 to 12 carbon atoms. Examples of C₆ to C₁₂ alkyl groups include groups —(CH₂)_(n)CH₃ wherein n is from 5 to 11, and branched alkyl groups including, methyl-pentyl, methyl-hexyl and dimethyl-hexyl such as 2,6-dimethylhexyl. A C₁ to C₄ alkyl group is a linear or branched alkyl group containing from 1 to 4 carbon atoms, for example, methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl or tert-butyl. A C₁ to C₄ alkyl group is typically a C₁ to C₂ alkyl group. A C₁ to C₂ alkyl group is methyl or ethyl, typically methyl. For the avoidance of doubt, where two alkyl groups are present, the alkyl groups may be the same or different.

As used herein, a C₃ to C₂₀ alkenyl group is a linear or branched alkenyl group containing from 3 to 20 carbon atoms and having one or more, e.g. one or two, double bonds. Typically a C₃ to C₂₀ alkenyl group is a C₄ to C₁₆ alkenyl group, e.g. a C₆ to C₁₂ alkenyl group. A C₆ to C₁₂ alkenyl group is a linear or branched alkenyl group containing from 6 to 12 carbon atoms and having one or more, e.g. one or two, double bonds. Examples of C₆ to C₁₂ alkenyl groups include hexenyl, heptenyl, octenyl, decenyl and undecenyl, methyl-hexenyl and dimethyl-hexenyl. For the avoidance of doubt, where two alkenyl groups are present, the alkenyl groups may be the same or different.

As used herein, a C₃ to C₂₀ alkynyl group is a linear or branched alkynyl group containing from 3 to 20 carbon atoms and having one or more, e.g. one or two, triple bonds. Typically a C₃ to C₂₀ alkynyl group is a C₄ to C₁₆ alkynyl group, e.g. a C₆ to C₁₂ alkynyl group. A C₆ to C₁₂ alkynyl group is a linear or branched alkynyl group containing from 6 to 12 carbon atoms and having one or more, e.g. one or two, double bonds. Examples of C₆ to C₁₂ alkynyl groups include hexynyl, heptynyl, octynyl, decynyl and undecynyl, methyl-hexynyl and dimethyl-hexynyl. For the avoidance of doubt, where two alkynyl groups are present, the alkynyl groups may be the same or different.

An alkyl, alkenyl or alkynyl group as used herein may be unsubstituted or substituted. Substituted alkyl, alkenyl or alkynyl groups typically carry from one to six, e.g. one, two or three, e.g. one substituent selected from halogen, OH, C₁ to C₄ alkoxy and —NR¹⁰R¹¹.

As used herein, a halogen is typically chlorine, fluorine, bromine or iodine and is preferably chlorine, bromine or fluorine.

As used herein, a C₁ to C₄ alkoxy group is typically a said C₁ to C₄ alkyl group attached to an oxygen atom. A C₁ to C₂ alkoxy group is methoxyl or ethoxy.

As used herein, a pharmaceutically acceptable salt is a salt with a pharmaceutically acceptable acid or base. Pharmaceutically acceptable acids include both inorganic acids such as hydrochloric, sulphuric, phosphoric, diphosphoric, hydrobromic or nitric acid and organic acids such as citric, fumaric, maleic, malic, ascorbic, succinic, tartaric, benzoic, acetic, methanesulphonic, ethanesulphonic, benzenesulphonic or p-toluenesulphonic acid. Pharmaceutically acceptable bases include alkali metal (e.g. sodium or potassium) and alkali earth metal (e.g. calcium or magnesium) hydroxides and organic bases such as alkyl amines, aralkyl amines and heterocyclic amines.

Lipid Altered Tunicamycin Analogues

The lipid altered tunicamycin analogues of the present invention are an oligosaccharide which is a compound according to Formula (I), or a pharmaceutically acceptable salt thereof,

In Formula (I), the stereochemistry is not limited. However, preferred oligosaccharides of Formula (I) have a structure according to Formula (II).

Compounds of formula (I) containing one or more chiral centre may be used in enantiomerically or diastereoisomerically pure form, or in the form of a mixture of isomers. Further, for the avoidance of doubt, the compounds of the invention may be used in any tautomeric form. Preferably, the compounds of formula (I) are those according to Formula (II), i.e. the compounds of formula (I) preferably have the stereochemistry as shown in Formula (II). Typically, the oligosaccharide described herein contains at least 50%, preferably at least 60, 75%, 90% or 95% of the compound having the stereochemistry of Formula (II). More preferably, the oligosaccharide described herein contains at least 98%, 99% or 99.5% of the compound having the stereochemistry of Formula (II). Thus, the compounds is preferably substantially optically pure.

In Formula (I), [Base] is a natural nucleobase selected from adenine, cytosine, guanine, thymine and uracil. Preferably, [Base] is a pyrimidine nucleobase. More preferably, the base is thymine (T) or uracil (U), with uracil (U) being most preferable.

In Formula (I), each R¹, which may be the same or different, is typically OH or —OPO(OH)₂, preferably each R¹ is OH.

In Formula (I), each R², which may be the same or different, is typically H or methyl, preferably each R² is H.

In Formula (I), R³ and R⁴, which may be the same or different, are typically H, OH, methyl, NH₂ or halogen, with H and OH being preferable. More preferably R³ and R⁴ are both H.

In Formula (I), each R⁵, which may be the same or different, is typically H or C₁ to C₂ alkyl, preferably each R⁵ is H.

In Formula (I), each R⁶, which may be the same or different, is typically OH, —NHCOCH₃ or —OPO(OH)₂. Each R⁶ is preferably OH.

In Formula (I), one or more R⁷ and/or one or more R⁸ is a group —NHC(O)R⁹; the remaining groups R⁷, which may be the same or different, are independently H, halogen, or C₁ to C₂ alkyl; and the remaining groups R⁸, which may be the same or different, are independently OH, halogen, —OPO(OH)₂, —OCO₂CH₃, —NHCOCH₃ or C₁ to C₂ alkoxy. Each remaining group R⁷ is preferably H or C₁ to C₂ alkyl, with H being most preferable. Each remaining group R⁸ is preferably OH, —NHCOCH₃ or —OPO(OH)₂, with OH being most preferable.

Each R¹⁰ and R¹¹, which may be the same or different, is typically H or C₁ to C₂ alkyl. Preferably, R¹⁰ and R¹¹ are H.

Typically, each R⁹ group is the same.

Typically, each R⁹ is C₃ to C₂₀ alkyl or C₃ to C₂₀ alkenyl. Alkyl groups, in particular n-alkyl groups, are preferred in one embodiment. Thus, R⁹ is a carbon chain of at least 3 carbon atoms. Preferably, R⁹ has at least 4 carbon atoms, more preferably at least 6 carbon atoms, still more preferably at least 7 carbon atoms. R⁹ is a carbon chain of no more than 20 carbon atoms, preferably no more than 16, more preferably no more than 12, still more preferably no more than 9 carbon atoms. R⁹ may therefore be an alkyl, alkenyl or alkynyl group, preferably an alkyl or alkenyl group, having from, for example, 3 to 20 carbon atoms, 4 to 16 carbon atoms, 6 to 12 carbon atoms, or 7 to 9 carbon atoms, such as 8 carbon atoms. R⁹ is preferably unsubstituted or is substituted by from 1 to 4 substituents, e.g. from 1 to 3 substituents such as one or two substituents. The substituents are preferably selected from halogen, OH, C₁ to C₄ alkoxy, and —NR¹⁰R¹¹. More preferably, the substituents are selected from halogen, OH and C₁ to C₂ alkoxy. Still more preferably, the substituents are selected from halogen and OH. Most preferably, R⁹ is unsubstituted.

In Formula (I), it is preferable that one of the R⁷ and/or R⁸ groups which are —NHC(O)R⁹ is bonded to the C2″ carbon (see Formula (IV) below). The C2″ carbon is the carbon atom adjacent to the C1″ carbon atom. The C1″ carbon atom is connected via oxygen to the sugar ring carrying R⁵ and R⁶ groups.

In Formula (I), it is preferable that the total number of R⁷ and R⁸ groups which are —NHC(O)R⁹ is from 1 to 3. Preferably, the total number of R⁷ and R⁸ groups which are —NHC(O)R⁹ is 1 or 2, and most preferably 1.

When one group R⁸ is —NHC(O)R⁹ it is preferable that the ring carrying groups R⁷ and R⁸ has a structure according to Formula (IV):

A preferred lipid altered tunicamycin analogue of the present invention is an oligosaccharide which is a compound according to Formula (I) or (II) above, or a pharmaceutically acceptable salt thereof, wherein:

-   -   [Base] is thymine (T) or uracil (U);     -   each R¹, which may be the same or different, is OH or —OPO(OH)₂;     -   each R², which may be the same or different, is H or methyl;     -   R³ and R⁴, which may be the same or different, are H, OH,         methyl, NH₂ or halogen;     -   each R⁵, which may be the same or different, is H or C₁ to C₂         alkyl;     -   each R⁶, which may be the same or different, is OH, —NHCOCH₃ or         —OPO(OH)₂;     -   one, two or three groups, preferably one group, selected from         the groups R⁷ and R⁸ is a group —NHC(O)R⁹; the remaining groups         R⁷, which may be the same or different, are independently H or         C₁ to C₂ alkyl; and the remaining groups R⁸ which may be the         same or different, are independently OH, —NHCOCH₃ or —OPO(OH)₂;     -   each R⁹ is the same or different and is, independently, C₄ to         C₁₆ alkyl or C₄ to C₁₆ alkenyl group which is unsubstituted or         is substituted by from 1 to 4 substituents selected from         halogen, OH, C₁ to C₄ alkoxy, and —NR¹⁰R¹¹; and     -   each R¹⁰ and R¹¹, which may be the same or different, is H or C₁         to C₂ alkyl.

A more preferred lipid altered tunicamycin analogue of the present invention is an oligosaccharide which is a compound according to Formula (III), or a pharmaceutically acceptable salt thereof,

wherein each R⁹, which may be the same or different, is defined as above. Preferably each R⁹ is the same. Preferably, in this embodiment, each R⁹ is C₆ to C₁₂ alkyl or C₆ to C₁₂ alkenyl, in particular C₆ to C₁₂ alkyl, preferably linear C₆ to C₁₂ alkyl. In one embodiment R⁹ is a linear C₇ to C₉ alkyl group. Typically, R⁹ is unsubstituted or is substituted by one or two substituents selected from halogen and OH. Most preferably, R⁹ is unsubstituted.

A particularly preferred lipid altered tunicamycin analogue of the present invention is an oligosaccharide which is a compound according to Formula (III), or a pharmaceutically acceptable salt thereof, wherein R⁹ is selected from

The compounds of the invention can, for example, be prepared according to the following general reaction sequence. A tunicamyl derivative may be derived from crude tunicamycin. Standard modifications can be employed to alter the structure of the tunicamyl derivative at this or subsequent stages in the synthesis. Derivatives may be produced by introduction of, for example, BOC (tert-butyloxycarbonyl) groups followed by base treatment. Acylation may also be used. Divergent intermediates containing the fully intact tunicamycin-derived core scaffold may be derived by the further introduction of BOC groups followed by mild basic cleavage. Lipids may be introduced to yield lipid-modified tunicamycin analogues.

The compounds of the present invention are therapeutically useful. The present invention therefore provides a lipid altered tunicamycin analogue of the formula (I), as defined above, or a pharmaceutically acceptable salt thereof, for use in treating the human or animal body. For the avoidance of doubt, the compounds of formula (I) can, if desired, be used in the form of solvates.

Also provided is a pharmaceutical composition comprising lipid altered tunicamycin analogue of the formula (I), as defined above, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent. Said pharmaceutical composition typically contains up to 85 wt % of a compound of the invention. More typically, it contains up to 50 wt % of a compound of the invention. Preferred pharmaceutical compositions are sterile and pyrogen free. Further, the pharmaceutical compositions provided by the invention typically contain a compound of the invention which is a substantially pure optical isomer.

As explained above, the compounds of the invention are useful in treating or preventing a bacterial infection. The present invention therefore provides a lipid altered tunicamycin analogue of the formula (I), as defined above, or a pharmaceutically acceptable salt thereof, for use in treating or preventing a bacterial infection. Also provided is a method for treating a subject suffering from or susceptible to a bacterial infection, which method comprises administering to said subject an effective amount of a lipid altered tunicamycin analogue of the formula (I), as defined above, or a pharmaceutically acceptable salt thereof. Further provided is the use of a lipid altered tunicamycin analogue of the formula (I), as defined above, or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in treating or preventing a bacterial infection.

In one aspect, the subject is a mammal, in particular a human. However, it may be non-human. Preferred non-human animals include, but are not limited to, primates, such as marmosets or monkeys, commercially farmed animals, such as horses, cows, sheep or pigs, and pets, such as dogs, cats, mice, rats, guinea pigs, ferrets, gerbils or hamsters. The subject can be any animal that is capable of being infected by a bacterium.

The bacterium causing the infection may be any bacterium expressing MraY or an analogue thereof. Typically the bacterium causing the infection expresses MraY. The bacterium may, for instance, be any bacterium that has a peptidoglycan component in the cell wall. The bacterium may be Gram-positive or Gram-negative. In a preferred instance the bacterium is Gram-positive. The bacterium may in particular be a pathogenic bacterium.

In one preferred instance, the bacterium may be one selected from a bacterium of the following Gram-positive bacteria families: Actinomyces, Bacillus (including Enterococcus), Clostridium, Corynebacterium, Listeria, Mycobacterium, Mycoplasma, Streptococcus and Staphylococcus (including MRSA). Examples of Gram-positive bacteria include Actinomyces israelii, Clostridium botulinum, Clostridium difficile, Clostridium perfringens, Clostridium tetani, Corynebacterium diptheriae, Enterococcus faecalis, Enterococcus faecium, Listeria monocytogenes, Mycobacterium avium, Mycobacterium tuberculosis, Mycobacterium leprae, Mycoplasma pneumoniae, Staphylococcus aureus, Staphylococcus epidermidis, Staphylococcus saprophyticus, Streptococcus agalactiae, Streptococcus pneumoniae and Streptococcus pyogenes.

In one preferred instance, the bacterium may be one selected from a bacterium of the following Gram-negative bacteria families: Acinetobacter, Bordetella, Borrelia, Brucella, Burkholderia, Campylobacter, Chlamydia, Chlamydophila, Enterobacter, Escherichia, Helicobacter, Hemophilus, Klebsiella, Legionella, Leptospira, Moraxella, Neisseria, Proteus, Pseudomonas, Salmonella, Serratia, Shigella, Treponema, Vibrio and Yersinia. Examples of Gram-negative bacteria include Acinetobacter baumannii, Bordetella pertussis, Borrelia burgdorferi, Brucella abortus, Brucella canis, Brucella melitensis, Brucella suis, Burkholderia cenocepacia, Campylobacter jejuni, Chlamydia pneumoniae, Chlamydia psittaci, Chlamydia trachomatis, Enterobacter cloacae, Escherichia coli, Francisella tularensis, Haemophilus influenzae, Helicobacter pylori, Klebsiella pneumoniae, Legionella pneumophila, Leptospira interrogans, Moraxella catarrhalis, Neisseria gonorrhoeae, Neisseria meningitidis, Proteus mirabilis, Pseudomonas aeruginosa, Rickettsia rickettsii, Salmonella enteritidis, Salmonella typhi, Salmonella typhimurium, Serratia marcescens, Shigella sonnei, Treponema pallidum, Vibrio cholerae and Yersinia pestis.

In a preferred embodiment, the bacterium is a Bacillus, Pseudomonas, or Mycobacterium. In another instance, the bacterium is a Streptococcus or Pseudomonas, particularly where the condition to be treated is pneumonia. In another instance the bacterium may be Shigella, Campylobacter or Salmonella, particularly where the condition to be treated is a food borne infection. Alternatively, the condition to be treated may be tetanus, typhoid fever, diphtheria, syphilis or leprosy. For instance, the bacterium may be one selected from the group Clostridium tetani, Salmonella typhi, Corynebacterium diptheriae, Treponema pallidum and Mycobacterium leprae. In another instance, the bacterium may be an opportunistic pathogen, and in a preferred instance may be selected from Pseudomonas aeruginosa, Burkholderia cenocepacia, and Mycobacterium avium. In a further instance, the bacterium may be Chlamydia, Mycobacterium or Brucella. In a further preferred instance, the bacterium is a Mycobacterium (including tuberculosis and leprae). In one instance the bacterium is Mycobacterium tuberculosis, particularly where the condition to be treated or prevented is tuberculosis. In further instances, the bacterium may be Chlamydia pneumoniae, Chlamydia trachomatis, Chlamydophila psittaci, Mycobacterium leprae, Mycobacterium tuberculosis or Mycoplasma pneumoniae.

The invention may be used to treat or prevent infections and conditions caused by any of the above-mentioned bacteria. In particular, the oligosaccharides described herein may be used in the treatment or prevention of pneumonia, food borne infections, tetanus, typhoid fever, diphtheria, syphilis, leprosy or tuberculosis. In particular, the oligosaccharides described herein may be used in the treatment or prevention of tuberculosis.

The lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof can be administered to the subject in order to prevent the onset of one or more symptoms of the bacterial infection. This is prophylaxis. In this embodiment, the subject can be asymptomatic. The subject is typically one that has been exposed to the bacterium. A prophylactically effective amount of the lipid altered tunicamycin analogue is administered to such a subject. A prophylactically effective amount is an amount which prevents the onset of one or more symptoms of the bacterial infection.

The lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof can be administered to the subject in order to treat one or more symptoms of the bacterial infection. In this embodiment, the subject is typically symptomatic. A therapeutically effective amount of the lipid altered tunicamycin analogue is administered to such a subject. A therapeutically effective amount is an amount effective to ameliorate one or more symptoms of the disorder.

The lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof may be administered in a variety of dosage forms. Thus, it can be administered orally, for example as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules. The lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof may also be administered parenterally, whether subcutaneously, intravenously, intramuscularly, intrasternally, transdermally or by infusion techniques. The lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof may also be administered as a suppository.

The lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof is typically formulated for administration with a pharmaceutically acceptable carrier or diluent. For example, solid oral forms may contain, together with the active compound, diluents, e.g. lactose, dextrose, saccharose, cellulose, corn starch or potato starch; lubricants, e.g. silica, talc, stearic acid, magnesium or calcium stearate, and/or polyethylene glycols; binding agents; e.g. starches, arabic gums, gelatin, methylcellulose, carboxymethylcellulose or polyvinyl pyrrolidone; disaggregating agents, e.g. starch, alginic acid, alginates or sodium starch glycolate; effervescing mixtures; dyestuffs; sweeteners; wetting agents, such as lecithin, polysorbates, laurylsulphates; and, in general, non toxic and pharmacologically inactive substances used in pharmaceutical formulations. Such pharmaceutical preparations may be manufactured in known manner, for example, by means of mixing, granulating, tableting, sugar coating, or film coating processes.

Liquid dispersions for oral administration may be syrups, emulsions and suspensions. The syrups may contain as carriers, for example, saccharose or saccharose with glycerine and/or mannitol and/or sorbitol.

Suspensions and emulsions may contain as carrier, for example a natural gum, agar, sodium alginate, pectin, methylcellulose, carboxymethylcellulose, or polyvinyl alcohol. The suspension or solutions for intramuscular injections may contain, together with the active compound, a pharmaceutically acceptable carrier, e.g. sterile water, olive oil, ethyl oleate, glycols, e.g. propylene glycol, and if desired, a suitable amount of lidocaine hydrochloride.

Solutions for injection or infusion may contain as carrier, for example, sterile water or preferably they may be in the form of sterile, aqueous, isotonic saline solutions. Pharmaceutical compositions suitable for delivery by needleless injection, for example, transdermally, may also be used.

In some embodiments, the invention provides an injectable composition comprising the lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof.

In one embodiment, the invention provides an injectable composition comprising the lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof, a buffer solution, an alcohol and optionally a surfactant. In this embodiment, the lipid altered tunicamycin analogue or pharmaceutically acceptable salt thereof is typically present in an amount of up to 5 mg/mL, for example from 0.001 to 4 mg/mL, e.g. 0.5 to 3 mg/mL. The buffer solution typically has a pH of approximately 7, such as from pH 6 to pH 8.5, preferably from pH 7 to pH 7.5. The buffer solution may be a phosphate buffer saline solution (PBS). The buffer solution usually forms the basis of the injectable composition. The amount of buffer solution is typically at least 50% of the solution by weight, for instance from 50% to 99.5%, e.g. from 70% to 95% by weight. The alcohol in the injectable composition is usually a C₁₋₆ alcohol such as methanol, ethanol or propanol. Preferably the alcohol is ethanol. The amount of alcohol in the injectable composition is usually less than 50% by weight, for example from 0.5% to 50%, e.g. from 5% to 30% by weight. Where the surfactant is present, the surfactant may be present in an amount of from 0.1% to 10% by weight, e.g. from 0.5% to 5% by weight. The surfactant may be, for example, Tween-80.

A therapeutically or prophylactically effective amount of the lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof is administered to a subject. The dose may be determined according to various parameters, especially according to the compound used; the age, weight and condition of the subject to be treated; the route of administration; and the required regimen. Again, a physician will be able to determine the required route of administration and dosage for any particular subject. A typical daily dose is from about 0.01 to 100 mg per kg, preferably from about 0.1 mg/kg to 50 mg/kg, e.g. from about 1 to 10 mg/kg of body weight, according to the activity of the specific inhibitor, the age, weight and conditions of the subject to be treated, the type and severity of the disease and the frequency and route of administration. Preferably, daily dosage levels are from 5 mg to 2 g.

The invention provides a pharmaceutical composition comprising a lipid altered tunicamycin analogue of the invention or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier. Such pharmaceutical compositions comprise a therapeutically or prophylactically effective amount of the lipid altered tunicamycin analogue or a pharmaceutically acceptable salt thereof and may further comprise instructions to enable the kit to be used in the methods described herein or details regarding which subjects the method may be used for.

The following Examples illustrate the invention. They do not however, limit the invention in any way. In this regard, it is important to understand that the particular assay used in the Examples section is designed only to provide an indication of antibacterial activity. There are many assays available to determine such activity, and a negative result in any one particular assay is therefore not determinative.

EXAMPLES Abbreviations

ACN acetonitrile Ac₂O acetic anhydride CFU colony forming unit

CLSI Clinical and Laboratory Standards Institute

DCM dichloromethane DIC N,N′-diisopropylcarbodiimide DMAP 4-dimethylaminopyridine DMEM Dulbecco's modified Eagle's medium DMF dimethylformamide

DSMZ Deutsche Sammlung von Mikroorganismen and Zellkulturen GmbH

EtOAc ethyl acetate FA formaldehyde FBS fetal bovine serum HPLC high performance liquid chromatography HRMS high resolution mass spectroscopy IC50 half maximal inhibitory concentration iPOH/iPrOH isopropanol IR infra-red (spectroscopy) LRMS low resolution mass spectroscopy MBC minimum bactericidal concentration

MH Mueller-Hinton

MIC minimum inhibitory concentration Mp melting point MraY phospho-N-acetylmuramoyl-pentapeptide transferase

NIH National Institute of Health

NMR nuclear magnetic resonance OD₆₀₀ optical density at a wavelength of 600 nm PBS phosphate buffered saline R_(f) retardation factor RT room temperature RTI relative therapeutic index SEM standard error of the mean TEA triethyl amine TFA trifluoroacetic acid THF tetrahydrofuran TLC thin layer chromatography

TM Tunicamycin

W water

General Considerations

Proton (¹H) nuclear magnetic resonance (NMR) (δH) spectra were recorded on Bruker DPX 200 (200 MHz), Bruker DPX 400 (400 MHz), Bruker DQX 400 (400 MHz), or Bruker AVC 500 (500 MHz) spectrometer. Carbon (¹³C) nuclear magnetic resonance spectra were recorded on Bruker DQX400 (100 MHz) or Bruker AVC 500 (125 MHz) with a ¹³C cryoprobe (125 MHz). Spectra were assigned using a combination of ¹H, ¹³C, HSQC, HMBC, COSY, and TOCSY. All chemical shifts were quoted on 6-scale in ppm, with residual solvent as internal standard. Coupling constants (J) are reported in Hertz (Hz). Infrared spectra were recorded on a Bruker Tensor 27 Fourier Transform spectrophotometer recorded in wavenumbers (cm⁻¹). Low-resolution mass spectra were recorded on a LCT Premier XE using electrospray ionization (ES). High-resolution mass spectra were recorded on a Bruker microTOF. Specific rotations were measured on PerkinElmer 241 polarimeter with path length of 1.0 dm and concentration (c) in g/100 mL. Thin layer chromatography (TLC) was performed on Merck EMD Kieselgel 60F₂₅₄ precoated aluminium backed plates. Reverse-phase thin layer chromatography (RF-TLC) was performed on Merck EMD Silica Gel RP-18 W F254s precoated glass backed plates. TLC and RF-TLC were visualized in combination of: 254/365 nm UV lamp; sulfuric acid (2 M in EtOH/W 1:1) [W=water]; ninhydrin (2% ninhydrin in EtOH); aqueous KMnO₄ (5% KMnO₄ in 1 M NaOH); aqueous phosphomolybdinc acid/Ce(IV) (2.5% phosphomolybdic acid hydrate, 1% cerium(IV) sulfate hydrate, and 6% H₂SO₄); or ammonium molybdate3 (5% in 2M H₂SO₄). Flash chromatography was carried out with Fluka Kiegselgel 60 220-440 mesh silica gel. All solvents (analytical or HPLC) used were purchased from Sigma Aldrich, Fisher Scientific, or Rathburn. Anhydrous solvents were purchased from Sigma Aldrich and stored over molecular sieves (<0.005% H₂O). Petrol refers to the fraction of petroleum ether having boiling point in the range of 40-60° C. Analytical (Synergi™ 4 μm Hydro-RP 80A 100×4.60 mm) and preparative (Synergi™ 4 μm Hydro-RP 80A 100×21.20 mm) reversed phase C18 column for HPLC were obtained from Phenomenex. Brine refers to saturated solution of NaCl.

Analytical Scale HPLC Analysis was Performed as Follows:

Analytical-scale HPLC analysis and preparative-scale HPLC purification were performed on an UltiMate 3000, and the resulting data was analysed using Chromeleon software.

Column: Phenomenex, Synergi 4u Hydro-RP 80 Å 100×4.60 mm 4 micron. Flow rate: 1 mL/min.; Solvent A: 5% ACN and 0.1% FA in H₂O; Solvent B: 0.1% FA in ACN; UV 260 nm. Eluent gradient (minutes/% B): 1.000/0.0; 25.000/100.0; 27.010; 100.0; 29.010/0.0; 35.010/0.0.

Preparative Scale HPLC Purification was Performed as Follows:

Column: Phenomenex, Synergi 4u Hydro-RP 80A 100×21.20 mm 4 micron. Flow rate: 12 mL/min.; Solvent A: 5% ACN and 0.1% FA in H₂O; Solvent B: 0.1% FA in ACN; UV 260 nm. Eluent gradient (minutes/% B): 1.000/0.0; 25.000/100.0; 27.010/100.0; 28.010/0.0; 35.010/0.0

BIOLOGICAL EXPERIMENTS

All prepared biological solutions and equipment, such as media, plastic and glassware, used in handling of the microbial cultures were autoclaved/sterilized at 121° C. for 20 minutes in LTE Scientific Ltd tabletop Touchclave® autoclave. All biological work was performed in a Bassaire laminar flow cabinet. Bacterial cultures were incubated in New Brunswick Scientific, Innova 42 Incubator Shaker Series. Centrifugation was performed in Thermo Scientific Heraeus Megafuge 40R centrifuge. Optical density was measured on BMG Labtech SPECTROstar Omega spectrophotometer or Amersham Bioscience Ultrospec 10. Water was deionized and passed through Millipore 0.22 μm filter prior to use. All human tissue culture work was carried out in a designated tissue culture room, with equipments and biosafety cabinet. Gloves and long-sleeve lab gown were worn at all times. Any bio-waste or consumable tissue culture materials were disposed in a designated auto-clave waste bin.

Mueller-Hinton (MH) broth (Oxoid) was prepared according to the manufacturer's procedure. Mueller-Hinton Agar (Oxoid) was prepared according to the manufacturer's procedure. Muller-Hinton agar plates were prepared according to CLSI standards. In this regard, Mueller-Hinton Agar (Oxoid) was prepared according to the manufacturer's procedure. 25 mL of the warm agar solution was transferred to 90 mm×16.2 mm plates via sterile pipette. The agar plate was cooled at room temperature for 15 minutes before use or storage at 4° C. up to two weeks. Stock solutions were prepared as 1.25 mg/mL or 1 mg/mL in MilliQ water or methanol, and stored at −20° C.

Bacteria used were as follows: [Test strain/(Gram+/−)/Description/Source]

-   -   Streptomyces chartreusis/+/NRRL3882/DSMZ     -   Bacillus subtilis EC1524/+/Tunicamycin sensitive strain/John         Innes Centre     -   Bacillus cereus/+/Test strain, ATCC 11778/DSMZ     -   Pseudomonas aeruginosa/−/Standard test strain, ATCC 27853/Thermo         Scientific     -   Mycobacterium tuberculosis/+/HR/NIH         Mammalian Cell Lines used were as follows:     -   HepG2 Human hepatocellular carcinoma cells     -   HEK293 Human embryonic kidney cells

Example 1: Synthesis of Lipid-Altered Tunicamycin Analogues

Lipid modified tunicamycin derivatives E1 to E7 and underlying scaffold compounds A to D were synthesized.

The following semi-synthetic scheme illustrates the reaction processes detailed below.

Tunicamycin (TM, 1)

Crude tunicamycin (TM) was isolated from S. chartreusis NRRL3882 fermentation culture by methanol extraction. Optimised growth and extraction processes allowed yields of 42±5 mg per litre of culture.

In one example, crude tunicamycin was isolated from a S. chartreusis NRRL3882 fermentation culture by methanol extraction (Hamill, 1980; Takatsuki et al., 1971). S. chartreusis spore stock (2 μL) was added to 50 mL of TYD media in a 250 mL spring coiled flask, and incubated at 28° C. and 200 rpm in a New Brunswick Series 25 shaker. After 36 h, aliquots of this culture (12×2 mL) was added to 12×1 L of TYD media including 6 g of glucose and 0.3 g of MgCl₂ in unbaffled 2 L conical flasks, which were subsequently incubated at 28° C. and 200 rpm in a New Brunswick Series 25 shaker. After 7 days, cells and supernatant were separated via decantation and centrifugation at 8500 rpm (Beckman Coulter Avanti J-25). Tunicamycin was extracted from both the centrifuged cells and supernatant. Tunicamycin in the supernatant was isolated by hydrophobic interaction chromatography. Amberlite XAD-16 was first preconditioned by washing with MeOH (×3) and then distilled water (×2). This preconditioned resin (15 g/L) was then added to the resulting supernatant and stirred for 2 h. The magnetic stirrer was then turned off and the XAD-16 resin was allowed to settle to the bottom of the flask, after which the majority of the supernatant was decanted and the remaining supernatant was removed by filtration. The collected resin was washed with water (200 mL) for 15 min and filtered through filter paper, and then stirred sequentially in MeOH (600 mL, 15 min), iPrOH (600 mL, 15 min) and MeOH (600 mL, overnight). The organic fractions were combined and concentrated in vacuo. The concentrated tunicamycin solution was aliquoted into four Falcon tubes and the volume adjusted to 40 mL with 1M HCl to precipitate tunicamycin. The insoluble precipitate was collected via centrifugation, re-dissolved in MeOH and then diluted with 400 mL of acetone. The acetone solution was kept at −20° C. overnight and the precipitated crude tunicamycin collected by filtration. Tunicamycin was also extracted from the cell pellet. The pellet was stirred in 1M aq. HCl (800 mL) for 30 min, after which the cells were collected by centrifugation at 9000 rpm (Beckman Coulter Avanti J-25). This process was repeated, after which the cell pellet was stirred in MeOH (400 mL) overnight. The cells were collected by filtration, resuspended in MeOH (400 mL) and stirred for a further 4 h. The MeOH fractions were combined, concentrated in vacuo, and tunicamycin precipitated with acetone (400 mL). Crude tunicamycin: TLC: R_(f) 0.3 in water/isopropanol/ethyl acetate (W/iPOH/EtOAc, 1:3:6); ¹H NMR (400 MHz, CD₃OD) δ ppm 0.89, 0.91 (2×s, 2×3 H, —CH(CH₃)₂), 1.14-1.66 (m, n×CH₂ ^(fatty acid)), 1.95 (s, 3H, —CH₃ ^(NHAc)), 3.36-4.05 (m, —CH₂ ^(sugar), CH^(sugar)), 4.10 (t, J=9.30 Hz, 1H, H-10′), 4.20 (t, J_(2′,1′)=5.80 Hz, 1H, H-2′), 4.59 (d, J_(11′,10′)=8.9 Hz, 1H, H-11′), 4.94 (d, J=3.6 Hz, 1H, H-1″), 5.77 (d, J_(5,6)=8.2 Hz, 1H, H-5^(uracil)), 5.95 (d, J_(1′,2′)=5.5 Hz, 1H, H-1′), 5.96 (d, J_(HC═CH trans)=15.4 Hz, 1H, ═CHC(O)—), 6.84 (dt, J_(HC═CH trans)=14.5 Hz, J=7.85 Hz, 1H, —CH₂HC═), 7.94 (d, J_(6,5)=8.2 Hz, 1H, H-6^(uracil)); LRMS m/z (ESI⁺): [(M+Na)⁺]=839 (18%), 853 (100%), 867 (92%), 881 (30%); (ESI⁻): [(M+Cl)⁻]=851 (20%), 865 (100%), 879 (94%), 893 (34%). Flanking peaks with mass±14 corresponded to 8×CH₂, 9×CH₂, 10×CH₂, and 11×CH₂. IR ν: 3325, 2925, 2360, 2342, 1665, 1376, 1234, 1093, 1025; LC/MS m/z (TOF MS ES⁺): 761, 775, 789, 803, 817, 831, 845, 859, 873, 887, 901. TOF-MS of crude tunicamycin extracted from the S. Chartruesis culture is shown in FIG. 6(a), while FIG. 6(b) shows the TOF-MS of a commercial tunicamycin standard obtained from Sigma Aldrich (Sigma Aldrich, retention time 14-19 min). Analysis of the quantity of tunicamycin obtained is shown in the Table below.

tunica- tunica- S. mycin mycin/ chartreusis Culture isolated^(a) Sample^(a) HPLC^(b) Purity^(c) Litre^(d) strain Vol. (L) (mg) (mg/mL) (mg/mL) (%) (mg/L) NRRL3882 12 687.3 1.25 1.0296 82.4 47.2 NRRL3882 24 1066.4 1.30 1.0201 78.5 34.9 NRRL3882 12 1483.1 1.40 0.4718 33.7 41.7 NRRL3882 11 891.1 1.40 0.7899 56.4 45.7 ^(a)Crude sample; ^(b)Crude sample concentration injected into HPLC for analysis. tunicamycins dissolved in methanol; ^(c)Determined by HPLC, based on a standardised curve; ^(d)Purity and Culture Vol. were taken in consideration into the initial tunicamycins isolated.

The average yield of tunicamycin per litre of culture, based on the tunicamycin/Litre information above, was 42±5 mg.

Fermentation of Streptomyces chartreusis cells was also repeated on a large scale to obtain tunicamycin. When performed on a large scale, the extraction was as follows. Sterile TYD media (2 g Tryptone, 2 g yeast extract, 6 g glucose and 30 mg MgCl₂.6H₂O per litre) was added to 4×500 mL conical spring flasks. Each flask was inoculated with 50 μl of the Streptomyces chartreusis spore stock (˜5×10⁷ spores) and incubated at 28° C. with shaking on a rotary shaker (250 RPM) for 4-5 days. The flasks were then used to inoculate 90 L of TYD media in a Bioflow5000 fermenter at the University of East Anglia Fermentation Suite. Cells were fermented at 32° C. with an air flow rate of 0.25 L/L/min for 5-7 days before being harvested. Tunicamycin was extracted from resulting mycelial cake as described above.

Heptaacetyl-tunicamyl-uracil, (2)

Crude TM (103 mg, 0.123 mmol) was suspended in 3 M aq. HCl (2 mL) and stirred under reflux at 105° C. for 3 hr. After 3 hr. the solvent was co-evaporated with toluene in vacuo. The residue was re-dissolved in dry pyridine (3 mL) and Ac₂O (2 mL). After 18 hr. of stirring at RT, TLC showed a product spot with R_(f) 0.3. After solvent was evaporated in vacuo, flash chromatography (MeOH/EtOAc, 1:19) afforded 2 (21 mg, 0.030 mmol, 25%).

N-acetyl-tunicamyl-uracil Compound A

Heptaacetyl-tunicamyl-uracil (2) (41.4 mg, 0.059 mmol) was dissolved in dry MeOH (5 mL), stirred and cooled to 0° C. NaOMe was added to make a final concentration of 0.01 M. Reaction was monitored by TLC (1:2:2, W/iPOH/EtOAc). Reaction was neutralized after 3 hr. with Dowex 50 W×8 H⁺ resin. Reaction solution filtered and concentrated in vacuo. Flash chromatography (W/iPOH/EtOAc, 1:2:2) afforded the product A (25.9 mg, 0.058 mmol, 98%).

Octa-O-acetyl-tunicamycin (4)

Crude TM (682 mg, 0.814 mmol) was dissolved in dry pyridine (5 mL) with an addition of Ac₂O (3 mL). After stirring at RT for 18 hours TLC (EtOAc) showed a major product at R_(f) 0.4 (4). The solvent was evaporated in vacuo and purified via flash chromatography (MeOH/DCM, 3:97) to afford the product 4 (782 mg, 0.667 mmol, 82%) as clear glass.

TLC: R_(f) 0.4 in methanol/dichloromethane (MeOH/DCM, 3:97); ¹H NMR (500 MHz, CD₃OD) δ ppm 7.48 (d, J_(6,5)=8.0 Hz, 1H, H-6^(uracil)), 6.83 (dt, J_(HC═CH trans)=14.2 Hz, J=7.3 Hz, 1H, C═CH—CH₂), 5.87 (d, J_(HC═CH trans)=15.5 Hz, 1H, C═CH—CO), 5.81 (d, J_(1′,2′)=5.1 Hz, 1H, H-1′), 5.75 (d, J_(5,6)=8.0 Hz, 1H, H-5^(uracil)), 5.56 (dd, J_(3′,2′)=6.1 Hz, J_(3′,4′)=5.5 Hz, 1H, H-3′), 5.51 (dd, J_(2′,1′)=J_(2′,3′)=5.3 Hz, 1H, H-2′), 5.26 (dd, J_(3″,2″)=10.6 Hz, J_(3″,4″)=9.9 Hz, 1H, H-3″), 5.27 (ddd, J_(5′,6′)=9.7 Hz, J_(5′,4′)=6.8 Hz, J=3.6 Hz, 1H, H-5′), 5.11 (dd, J_(8′,9′)=9.7 Hz, J_(8′,7′)=7.3 Hz, 1H, H-8′), 5.07 (app t, J_(4″,5″)=11.3 Hz, J_(4″,3″)=3.2 Hz, 1H, H-4″), 5.03 (dd, J_(9′,10′)=3.6 Hz, J_(9′,8′)=3.2 Hz, 1H, H-9′), 4.98 (d, J_(1″,2″)=4.9 Hz, 1H, H-1″), 4.75 (d, J_(11′,10′)=8.4 Hz, 1H, H-11′), 4.33 (dd, J_(6a″,6)b″=11.1 Hz, J_(6″,5″)=3.9 Hz, 1H, H-6″), 4.34 (dd, J_(10′,9′)=4.6 Hz, J_(10′,11)′=3.6 Hz, 1H, H-10′), 4.32 (ddd, J_(5″,4″)=10.4, J_(5″,6″)=2.9 Hz, J_(5″,6″)=2.2 Hz, 1H, H-5″), 4.20 (dd, J_(4′,3′)=7.7 Hz, J_(4′,5′)=3.6 Hz, 1H, H-4′), 4.19 (dd, J_(2″,3″)=7.2 Hz, J_(2″,1″)=3.1 Hz, 1H, H-2″), 4.19 (dd, J_(6a″,6b″)=14.2 Hz, J_(6″,5″)=2.6 Hz, 1H, H-6″), 3.92 (ddd, J=9.4 Hz, J_(7′,6′)=3.8 Hz, J_(7′,8′)=3.1 Hz, 1H, H-7′), 2.22 (s, 3H, CH₃ ^(Ac)), 2.17 (m, 2H, —CH₂CH═C), 2.14 (s, 6H, 2×CH₃ ^(Ac)), 2.10 (s, 3H, CH₃ ^(Ac)), 2.06 (m, 2H, H-6′), 2.04, 2.03, 1.98, 1.95, 1.89 (5×s, 5×3 H, 5×CH₃ ^(Ac)), 1.78 (ddd, J_(6b′,a)′=14.8 Hz, J_(6′,5′)=8 Hz, J_(6′,7′)=3.3 Hz, 1H), 1.55 (spt, J=6.7 Hz, 1H, —CH(CH₃)₂), 1.46 (quin, J=6.8 Hz, 2H, —CH₂CH₂CH═C), 1.23-1.37 (m, 14H, —CH₂ ^(acyl)), 1.18 (dt, J=13.1, 7.0 Hz, 2H, CH₂CH(CH₃)₂), 0.91, 0.89 (2×s, 2×3 H, —CH(CH₃)₂); ¹³C NMR (126 MHz, CD₃OD) δ ppm 173.2, 172.4, 172.3, 172.3, 172.0, 171.7, 171.5, 171.3, 171.2 (C═O^(Ac), C═O^(NHAc)), 169.5 (C═O^(acyl)), 165.9 (C-4 C═O), 151.8 (C-2 C═O), 147.7 (C═CH—CH₂), 143.4 (C-6^(uracil)), 124.2 (C═CH—CO), 103.5 (C-5^(uracil)), 101.6 (C-11′), 100.0 (C-1″), 91.1 (C-1′), 84.1 (C-4′), 73.5 (C-2′), 72.2 (C-3″), 72.2 (C-9′), 71.7 (C-7′), 70.9 (C-3′), 70.8, 70.3 (C-5′, C-8′), 69.8 (C-5″), 69.7 (C-4″), 63.0 (C-6″), 52.6 (C-2″), 51.8 (C-10′), 40.3 (—CH₂CH(CH₃)₂), 33.2 (—CH₂CH═C), 33.1 (C-6′), 30.3-31.1 (5×-CH₂ ^(acyl)), 29.4 (—CH₂CH₂CH═C), 29.2 (—CH(CH₃)₂), 28.6 (—CH₂ ^(acyl)), 23.0, 23.1 (—CH(CH₃)₂), 22.9 (—CH₃ ^(NHAc)), 21.1 (—CH₃ ^(Ac)), 20.7 (2×-CH₃ ^(Ac)), 20.6, 20.6, 20.6, 20.6, 20.3 (5×-CH₃ ^(Ac)); IR ν: 2927, 2361, 2341, 1745, 1696, 1540, 1369, 1219, 1031; MS m/z (ESI⁺): 1203 [(M+Na)⁺, 100%]; (ESI⁻): 1179 [(M+Cl)⁻, 100%]. Flanking peaks with mass±14 corresponded to 8×CH₂, 9×CH₂, 10×CH₂, and 11×CH₂. Full assignment was not possible due to the presence homologues with mass±14.

Tri-N-(tert-butoxylcarbonyl)-octa-O-acetyl-tunicamycin (5)

In order to cleave the lipid chain, the tert-butoxylcarbonyl (Boc) protecting group was added to the secondary amides at positions 3, 10′, and 2″ to afford the tri-N-Boc-octa-O-acetylated tunicamycins. Amide cleavage usually involves the use of a strong acid or base and high temperatures, but these harsh conditions would be unsuitable to use in the presence of the uridine moiety as they would degrade the tunicamycins. Several methodologies have been published on how to remove the highly stable and unreactive acetyl group. One of them is Kunieda's mild N-bocylation methodology. Attachment of Boc group to the secondary amide increases the electrophillicity of carbonyl, allowing the acetyl group to be readily cleaved in the presence of a base.

In one instance of the formation of (5), octa-O-acetyl-tunicamycin 4 (101 mg, 0.086 mmol) was dissolved in dry THF (1.5 mL) with the addition 4-(dimethylamino)pyridine (2.10 mg, 0.017 mmol) and di-tert-butyl dicarbonate (750 mg, 3.44 mmol) with 10 eq. added over time. The reaction flask was fitted over an oven dried condenser and heated to 60° C. with stirring. After 36 hr. TLC (EtOAc/Petrol, 6:4) showed R_(f) 0.3 and 0.1. The reaction was cooled and the solvent was evaporated in vacuo. Flash chromatography (EtOAc/Petrol, 6:4) afforded the product 5 (67.1 mg, 0.045 mmol, 53%) as yellow glass.

In another instance, octa-O-acetyl-tunicamycin 4 (101 mg, 0.086 mmol) was dissolved in dry THF (1.5 mL) with the addition of 4-(dimethylamino)pyridine (10.5 mg, 0.086 mmol) and di-tert-butyl dicarbonate (187.7 mg, 0.86 mmol). The reaction mixture was heated to 60° C. with stirring for 4 h, and subsequently another portion of di-tert-butyl dicarbonate (187.7 mg, 0.86 mmol) was added to the reaction mixture, with stirring continued for an additional 2 h. After a total of 6 h, the reaction mixture was checked by TLC (EtOAc/Petrol, 6:4). This which showed the formation of two products:

Compound 5 (R_(f) 0.3) and tunicamycin-8OAc-2Boc (R_(f) 0.1). The reaction mixture was concentrated in vacuo and purified by flash column chromatography (EtOAc/Petrol, 6:4). Compound 5 (31.1 mg, 0.021 mmol, 25%) was obtained as a yellow glass and tunicamycin-8OAc-2Boc (52.4 mg, 0.038 mmol, 44%) as a yellow oil; compound 5: TLC: R_(f) 0.5 in ethyl acetate/petrol (EtOAc/Petrol, 6:4); ¹H NMR (500 MHz, CDCl₃) δ ppm 7.48 (d, J_(6,5)=8.0 Hz, 1H, H-6^(uracil)), 6.89 (dt, J_(HC═CH trans)=15.1 Hz, J=6.9 Hz, 1H, C═CH—CH₂), 6.82 (dt, J_(HC═CH trans)=14.5 Hz, J=7.6 Hz, 1H, C═CH—CH₂), 6.39 (d, J_(HC═CH trans)=15.1 Hz, 1H, C═CHCO), 6.27 (d, J_(HC═CH trans)=15.4 Hz, 1H, C═CH—CO), 6.11 (m, 1H, C—H^(anomeric)), 5.85 (m, 1H, CH^(anomeric), H-5^(uracil)), 5.83 (d, J=8.2 Hz, 1H, H-5^(uracil)), 5.61 (dd, J=11.5 Hz, J=3.3 Hz, 1H), 5.53 (dd, J=11.3 Hz, J=3.5 Hz, 1H), 5.49 (d, J=8.2 Hz, 1H), 5.43 (m, 1H), 5.29-5.35 (m, 1H), 5.09-5.25 (m, 4H), 5.01-4.10 (m, 1H), 4.99 (d, J=9.1 Hz), 4.94 (dd, J=11.5 Hz, J=3.3 Hz, 1H), 4.91 (s, 1H), 4.52-4.60 (m, 1H), 4.30-4.39 (m, 1H), 4.17 (d, J=10.4 Hz, J=2.2 Hz, 1H), 4.05-4.10 (m, 1H), 3.76 (dd, J=8.8 Hz, J=3.5 Hz, 1H), 3.68 (dd, J=9.9 Hz, J=2.0 Hz, 1H), 2.34 (s, 1H), 2.29 (s, 2H, CH₃ ^(NHAc)), 2.27 (s, 1H, CH₃ ^(NHAc)), 1.87-2.22 (m, 24H, 8×CH₃ ^(Ac)), 1.59, 1.56, 1.55, 1.53, 1.52 (5×s, 27H, 9×CH₃ ^(Boc)), 1.40 (m, 13H), 1.08-1.18 (m, 2H, CH₂ ^(acyl)), 0.86, 0.85 (2×s, 2×3 H, CH₃ ^(acyl)); ¹³C NMR (126 MHz, CD₃OD) δ ppm 177.4, 177.5, 170.8, 170.7, 170.1, 169.9, 169.7, 169.6, 169.5, 169.4, 169.1 (C═O), 168.2 (C-4 C═O), 159.8 (C-2 C═O), 153.0, 152.9, 157.7, 152.7, 152.1, 148.3, 148.1, 147.3, 139.1, 139.0, 138.9 (C═CH—CH₂, C-6^(uracil)), 124.4, 123.9 (C═CH—CO), 103.5, 103.2 (C-1″), 97.8, 87.7, 86.9, 87.0, 86.9, 86.3, 82.4, 82.3, 72.1, 70.4, 70.2, 70.1, 69.6, 69.5, 69.4, 69.2, 69.1, 68.8, 68.0, 67.9, 61.5, 61.4, 57.657.0, 54.8, 39.0, 38.5, 36.6, 34.3, 32.7, 32.5, 32.4, 31.9, 29.9, 29.6, 29.5, 29.4, 29.3, 29.2, 28.2, 28.0, 27.9, 27.8, 27.6, 27.4, 22.6, 20.9, 20.9, 20.7, 20.6, 20.5, 20.4 (C-1′), 84.1 (C-4′), 73.5 (C-2′), 72.2 (C-3″), 72.2 (C-9′), 71.7 (C-7′), 70.9 (C-3′), 70.8, 70.3 (C-5′, C-8′), 69.8 (C-5″), 69.7 (C-4″), 63.0 (C-6″), 52.6 (C-2″), 51.8 (C-10′), 40.3 (—CH₂CH(CH₃)₂), 33.2 (—CH₂CH═C), 33.1 (C-6′), 30.3-31.1 (5×C, 5×-CH₂ ^(acyl)), 29.4 (—CH₂CH₂CH═C), 29.2 (—CH(CH₃)₂), 28.6 (—CH₂ ^(acyl)), 23.0, 23.1 (2×C, —CH(CH₃)₂), 22.9 (—CH₃ ^(NHAc)), 21.1 (—CH₃ ^(Ac)), 20.7 (2×C, 2×-CH₃ ^(Ac)), 20.6, 20.6, 20.6, 20.6, 20.3 (5×C, 5×-CH₃ ^(Ac)) IR ν: 2928, 2361, 2341, 1743, 1686, 1369, 1218, 1143, 1029; LRMS m/z (ESI⁺): 1503 [(M+Na)⁺, 100%]; (ESI⁻): 1515 [(M+Cl)⁻, 100%]. Flanking peaks with mass±14 corresponded to 8×CH₂, 9×CH₂, 10×CH₂, and 11×CH₂.

10′,2″-Di-N-Boc-α-D-glucosamine-(1″-11′)-tunicamyl uracil Compound B

In one instance, tri-N-(tert-butoxylcarbonyl)-octa-O-acetyl-tunicamycin 5 (134 mg, 0.091 mmol) was dissolved in MeOH:H₂O (v/v, 1:1) with the addition of TEA (25 equiv. 2.27 mmol, 317 The reaction was heated to 71° C. The reaction progress was monitored by TLC (1:2:6, W/iPOH/EtOAc). Reaction was complete after 43 hours. The crude product was purified by preparative scale HPLC and afforded the product B (36.4 mg, 0.047 mmol, 52%) as white amorphous powder.

In another instance, tri-N-(tert-butoxylcarbonyl)-octa-O-acetyl-tunicamycin 5 (134 mg, 0.091 mmol) was dissolved in MeOH:H₂O (v/v, 3:1) with the addition of TEA (25 equiv. 2.27 mmol, 317 μl). The reaction mixture was heated to 71° C. and reaction progress monitored by TLC (1:2:6, W/iPrOH/EtOAc). After 43 h the mixture was directly purified by preparative scale HPLC (retention time 9.5 min). Product containing fractions were pooled and lyophilized to afford Compound B (36.4 mg, 0.047 mmol, 52%) as white amorphous powder; TLC: R_(f) 0.3 in water/isopropanol/ethyl acetate (W/iPOH/EtOAc, 1:2:6); R_(f)=0.3 (H₂O/iPrOH/EtOAc, 1/2/7); [α]_(D) ²⁰=+54.9±0.3 (c 1, MeOH); Mp (amorphous) 177.4-181.2° C.; ¹H NMR (500 MHz, CD₃OD) δ ppm 7.91 (d, J=8.1 Hz, 1H, H-6), 5.93 (d, J=5.9 Hz, 1H, H-1′), 5.75 (d, J=8.1 Hz, 1H, H-5), 4.99 (s, 1H, H-1″), 4.70 (d, J=7.9 Hz, 1H, H-11′), 4.24 4.16 (m, 2H, H-2′, H-3′), 4.05-3.97 (m, 2H, H-5′, H-5″), 3.86 (t, J=3.3 Hz, 1H, H-4′), 3.81 (dd, J=11.7, 1.8 Hz, 1H, H-6″), 3.77-3.65 (m, 3H, H-7′, H-9′, H-6″), 3.64 (d, J=3.1 Hz, 1H, H-8′), 3.62 (d, J=4.9 Hz, 2H, H-2″, H-3″), 3.49 (t, J=9.6 Hz, 1H, H-10′), 3.37-3.33 (m, 1H, H-4″), 2.12-2.05 (m, 1H, H-6′), 1.57-1.49 (m, 1H, H-6′), 1.47 (s, 9H, CH₃), 1.45 (s, 9H, CH₃); ¹³C NMR (126 MHz, CD₃OD) δ ppm 166.2 (C-4), 158.7 (C═O^(Boc)), 158.5 (C═O^(Boc)), 152.6 (C-2), 142.8 (C-6), 103.1 (C-5), 101.4 (C-11′), 100.6 (C-1″), 89.7 (C-1′), 89.5 (C-4′), 80.7 (C—(CH₃)₃), 80.3 (C—(CH₃)₃), 75.5 (C-2′), 74.5 (C-5″), 73.6 (C-3″), 72.7, 72.6, 72.4 (C-7′, C-9′, C-4″), 72.3 (C-8′), 70.9 (C-3′), 68.4 (C-5′), 63.2 (C-6″), 56.6 (C-4″), 55.8 (C-10′), 35.9 (C-6′), 29.1 ((CH₃)₃), 28.8 ((CH₃)₃); IR (neat) ν: 3367 (N—H, O—H), 2979 (═C—H), 2930 (—C—H), 1684 (C═O); LRMS m/z (ESI⁺): 789 [(M+Na)⁺, 100%]; FIRMS m/z (ESI⁺): calc. C₃₁H₅₀N₄O₁₈Na (M+Na)⁺=789.3012, found 789.3017.

α-D-N-acetylglucosamine-(1″-11′)-N-acetyl tunicamyl uracil Compound C

In one instance, compound 5 (127 mg, 0.086 mmol) was dissolved in dry MeOH (5 mL), stirred and cooled to 0° C. NaOMe was added to make final concentration of 0.01 M, and monitored by TLC (1:3:6, W/iPOH/EtOAc). The reaction was neutralized after 4 hr. with Dowex 50 W×8 H⁺ resin. Then filtered and concentrated in vacuo, and redissolved in TFA (1 mL) and stirred at RT for 1 hr. TFA was coevaporated with toluene and then redissolved in MeOH (5 mL) with the addition of Ac₂O (1 mL). Reaction was stirred at RT for 12 hr. and neutralized to pH 6-7 with Dowex Marathon A ⁻OH resin, and stirred for additional 1 hr. Reaction solution was filtered and purified via flash chromatography (W/iPOH/EtOAc, 1:2:2) to afford N^(11′)-acetyl-N^(11′)-deacyl-tunicamcyin C (13.1 mg, 0.020 mmol, 23%) as yellow glass.

In another instance, compound 5 (127 mg, 0.086 mmol) was dissolved in dry MeOH (5 mL) and cooled to 0° C. NaOMe was added to a final concentration of 0.01 M and reaction progress monitored by TLC (1:3:6, W/iPOH/EtOAc). The reaction was neutralized after 4 h by addition of Dowex 50 W×8 H⁺ resin in parts until pH 7. The mixture was then filtered, the resin washed with methanol and the combined organics and concentrated in vacuo. The resulting solid was dissolved in TFA (1 mL) and stirred at RT for 1 h. The TFA was coevaporated with toluene and the crude material then redissolved in MeOH (5 mL) and Ac₂O (1 mL). The reaction mixture was stirred at RT for 12 h, neutralized to pH 6-7 with Dowex Marathon A—OH resin and stirred for an additional 1 h. The reaction mixture was filtered, concentrated in vacuo and purified by flash column chromatography (W/iPOH/EtOAc, 1:2:2) to afford compound C (13.1 mg, 0.020 mmol, 23%) as yellow glass; TLC: R_(f) 0.3 (W/iPOH/EtOAc, 1:2:2); [α]_(D) ²³=+50.7 (c=0.7, H₂O); ¹H NMR (500 MHz, CD₃OD) δ ppm 7.76 (d, J_(6,5)=7.9 Hz, 1H, H-6^(uracil)), 5.84 (d, J_(1′,2′)=7.9 Hz, 1H, H-1′), 5.83 (d, J_(5,6)=5.4 Hz, 1H, H5^(uracil)), 4.98 (d, J_(1″,2″)=3.5 Hz, 1H, H-1″), 4.58 (d, J_(11′,10)=8.5 Hz, 1H, H-6^(uracil)), 4.25 (dd, J_(2′,1′)=5.4 Hz, J_(2′,3′)=9.1 Hz, 1H, H-2′), 4.22 (dd, J_(3′,4′)=3.5 Hz, J_(3′,2′)=5.7 Hz, 1H, H-3′), 4.08-4.03 (m, 2H, H-4′, H-5′), 3.87 (dd, J_(10′,9′)=10.7 Hz, J_(10′,11′)=8.5 Hz, 1H, H-10′), 3.82-3.82 (m, 1H, H-4″), 3.80 (dd, =3.8 Hz, J_(2″,3″)=10.7, 1 H, H-2″), 3.77 (d, J=10.1 Hz, 1H, H-7′), 3.73-3.67 (m, 2×1 H, H-8′, H-6″), 3.70 (dd, J_(3″,2)″=10.7 Hz, J_(3″,4″)=3.2 Hz, 1H, H-3″), 3.68-3.41 (m, 2H, H-6″, H-9′), 3.44 (app t, J_(5″,6a″)=9.8 Hz, 1H, H-5″), 1.98, 1.94 (2×s, 2×3H, 2×-CH₃ ^(NHAc)), 1.94 (dd, J_(6b′,6a)′=6.6 Hz, J_(6b′,5′)=3.2 Hz, 1H, H-6′), 1.57 (app t, J_(6a′,6b′)=J_(6a′,5′)=13.2 Hz, 1H, H-6a′); ¹³C NMR (126 MHz, CD₃OD) δ ppm 174.5, 174.1 (C═O^(NHAc)), 166.2 (C-4, C═O), 151.8 (C-2, C═O), 141.9 (C-6^(uracil)), 102.5 (C-5^(uracil)), 99.8 (C-11′), 98.3 (C-1″), 88.5 (C-1′), 87.2 (C-4′), 73.4 (C-2′), 72.6 (C-4″), 71.3 (C-7′), 71.1, 70.4, 69.8 (C-3″, C-8′, C-9′), 69.6 (C-5″), 68.9 (C-3′), 67.0 (C-5′), 60.4 (C-6″), 53.4 (C-2″), 52.8 (C-10′), 33.5 (C-6′), 22.2, 22.1 (2×-CH₃ ^(NHAc)); IR (neat) ν: 3344, 2362, 2341, 2110, 1636, 1371, 1216; LRMS m/z (ESI⁺): 673.26 [(M+Na)⁺, 23%]; (ESI⁻): 649.23 [(M−H)⁻, 100%]; HRMS m/z (ESI+): calc. for C₂₅H₃₈N₄NaO₁₆ (M+Na)⁺=673.2175, found 673.2195.

α-D-glucosamine-(1″-11′)-tunicamyl uracil dihydrochloride Compound D

In one instance, 10′,2″-Di-N-Boc-α-D-glucosamine-(1″-11′)-tunicamyl uracil Compound B (64.6 mg, 0.085 mmol) was dissolved in DCM (1 mL) and TFA (50 equiv. 323 μL). The reaction was stirred at room temperature for 1 hr. The reaction progress was monitored by TLC (1:2:2, W/iPOH/EtOAc). When the reaction was complete, the reaction mixture was concentrated in vacuo and dried. The dried crude product was washed twice with H₂O and DCM. Aqueous fraction was collected, concentrated in vacuo and dried. The dried crude product was redissolved in 1 M HCl (1 mL) and stirred for 1 hr. at room temperature. The product D was obtained after lyophilisation, resulted in 93% yield (50 mg, 0.078 mmol).

In another instance, to a solution of Compound B (1.50 mg, 0.002 mmol) in DCM (120 μL) was added TFA (0.393 mmol 30 μL). The reaction mixture was stirred at room temperature for 1 h, with reaction progress monitored by TLC (1:2:2, W/iPOH/EtOAc). When the reaction was complete, the reaction mixture was concentrated in vacuo. The crude product was washed twice with H₂O and DCM, the aqueous fraction collected and concentrated in vacuo. The dried crude product was then redissoved in 1 M HCl (1 mL), stirred for 1 h at room temperature and lyophilized to yield the product D (1.20 mg, 99%). [α]_(D)20=+60.1±0.2 (c 1, H₂O); ¹H NMR (700 MHz, D₂O) δ ppm 7.82 (d, J=8.2 Hz, 1H, H-6), 5.87 (d, J=8.2 Hz, 1H, H-5) 5.86 (d, J=5.3 Hz, 1H, H-1′), 5.53 (d, J=3.4 Hz, 1H, H-1″), 5.00 (d, J=8.3 Hz, 1H, H-11′), 4.31-4.26 (m, 2H, H-2′, H-3′), 4.06 (td, J=2.6, 11.1 Hz, 1H, H-5′), 3.94 (dd, J=3.3, 11.0 Hz, 1H, H-9′), 3.92-3.87 (m, 3H, H-7′, H-3″, H-5″), 3.84 (d, J=3.2 Hz, 1H, H-8′), 3.79 (dd, J=3.8, 12.5 Hz, 1H, H-6″), 3.70 (dd, J=2.2, 12.4 Hz, 1H, H6″), 3.57 (t, J=9.6 Hz, 1H, H-4″), 3.39 (dd, J=3.5, 10.8 Hz, 1H, H-2″), 3.31 (dd, J=8.4, 11.0 Hz, 1H, H-10′), 1.97 (ddd, J=2.0, 10.4, 14.6 Hz, 1H, H-6′), 1.70-1.64 (dtd, J=2.8, 11.2 Hz, 1H, H-6′); ¹³C NMR (176 MHz, CD₃OD) δ ppm 166.17 (C-4), 151.8 (C-2), 142.0 (C-6), 102.4 (C-5), 99.4 (C-11′), 97.0 (C-1″), 88.7 (C-1′), 86.9 (C-4′), 73.4 (C-2′), 73.2 (C-5″), 71.8 (C-7″), 69.5 (C-8′), 69.3 (C-3″), 69.2 (C-9′), 68.9 (C-4′), 68.7 (C-3′), 66.9 (C-5′), 59.8 (C-6″), 53.8 (C-2″), 53.0 (C-10′), 33.3 (C-6′); IR (neat) ν: 3295 (N—H, O—H), 3057 (═C—H), 2922 (—C—H), 1673 (C═O), 1263 (C—N), 1109 (C—O), 1064 (C—O); LRMS m/z (ESI⁺): 567 [(M+H)⁺, 100%]; HRMS m/z (ESI⁺): calc. C₂₁H₃₅N₄O₁₄ (M+H)⁺=567.2144, found 567.2136.

General Protocol for Preparing Tunicamycin Analogues

Methods for preparing the tunicamycin analogues E1, E2, E3, E4, E5, E6 and E7 are described hereafter. An exemplary general protocol for preparation of these and any other tunicamycin analogues was as follows. HATU (2.5 equiv) was added to a solution of the appropriate carboxylic acid (2.5 equiv), EDC (2.5 equiv) and DIPEA (2.5 equiv) in dry DMF. The reaction mixture was stirred at RT for 10 min, followed by the addition of Compound D (1 equiv) and DIPEA (2.5 equiv). The reaction mixture was stirred at RT for 2˜4 h, diluted with a mixture of ACN/iPOH/Water (1:1:1) and purified by preparative HPLC.

Di-N-citronoyl-tunicamycin (E1)

(S)-(−)-citronellic acid (5.0 μL, 0.027 mmol, 2.5 equiv) and DIC (4.2 μL, 0.027 mmol, 2.5 equiv) were added to DMF (0.25 mL) with the addition of TEA (2 μL) and DMAP (2.7 mg, 0.022 mmol, 2 equiv.) and stirred at room temperature for one hour. Then, α-D-glucosamine (1″-11′)-tunicamyl uracil dihydrochloride Compound D (7 mg, 0.11 mmol) was dissolved in DMF (0.25 mL) with the addition of TEA (4.1 μL), and added to the citronellic acid reaction mixture. TEA was added to final of 4 equivalents. The reaction mixture was stirred at room temperature. The reaction progress was checked by TLC (1/3/6, H₂O/iPrOH/EtOAc) and HPLC. The reaction was stopped after 68 hours. The product was purified by HPLC, eluted at 14 min. The lyophilised product was washed with DCM and MilliQ water and resulted in 5.1 mg of the final product, 54% yield. R_(f)=0.4 (1/3/6, H₂O/iPrOH/EtOAc); [α]_(D) ²⁰=+45.2±0.2 (c 0.4, MeOH); ¹H NMR (500 MHz, MeOD) δ ppm 7.91 (d, J=8.1 Hz, 1H, H-6), 5.92 (d, J=5.9 Hz, 1H), H-1′), 5.75 (d, J=8.1 Hz, 1H, H-5), 5.11 (td, J=7.0, 1.0 Hz, 2H, H-5′″), 4.96 (d, J=3.4 Hz, 1H, H-1″), 4.58 (d, J=8.5 Hz, 1H, H-11′), 4.24-4.15 (m, 2H, H-2′, H-3′), 4.06-3.95 (m, 3H, H-5′, H-10′, H-5″), 3.91 (dd, J=10.6, 3.5 Hz, 1H, H-2″), 3.87-3.80 (m, 2H, H-4′, H-6″), 3.76 (appt dd, J=9.5, 1.9 Hz, 1H, H-7′), 3.71 3.60 (m, 4H, H-8′, H-9′, H-3″, H-6″), 3.33 (appt d, J=9.4 Hz, 1H, H-4″), 2.24 (m, 2H, H-1′″), 2.17-1.88 (m, 9H, H-6′, H-1′″, H-2″, H-4″), 1.67 (s, 6H, H-7″), 1.61 (s, 6H, H-8″), 1.52 (m, 1H, H-6′), 1.37 (m, 2H, H-3″), 1.23 (m, 2H, H-3″), 0.96 (d, J=6.4 Hz, 6H, H-9′″); ¹³C NMR (126 MHz, MeOD) δ ppm 176.64, 176.02, (2C, —N—C═O aliphatic chain), 166.18 (C-4), 152.63 (C-2), 142.78 (C-6), 132.31, 132.26 (2C, C-6″), 125.57, 125.50 (2C, C-5′″), 103.05 (C-5), 101.59 (C-11′), 99.99 (C-1″), 89.82 (C-1′), 89.62 (C-4′), 75.55 (C-2′), 74.37 (C-5″), 73.11, 73.00 (2C, C-8′, C-9′), 72.74 (C-4″), 72.48 (C-7′), 72.19 (C-3″), 70.86 (C-3′), 68.34 (C-5′), 63.23 (C-6″), 54.73 (C-2″), 54.36 (C-10′), 45.39, 44.91 (2C, C-1′″), 38.60, 38.50 (2C, C-3′″), 35.94 (C-6′), 31.78, 31.67 (2C, C-2′″), 26.66, 26.63 (2C, C-4″), 25.94 (C-7″), 19.65 (C-9″), 17.83 (C-8′″); IR (neat) ν: 3291 (O—H), 2966 (C—H), 2928 (C—H), 1700 (C═O), 1638 (C═O), 1541 (C═C), 1092 (C—N); LRMS m/z (ESI⁻): 915 [(M+FA-H)⁻, 100%]; HRMS m/z (ESI⁺): calc. C₄₁H₆₅N₄O₁₆ (M−H)⁻=869.4401, found 869.4407. (H-4″ signal in the 1H NMR spectrum observed to be partially overlapped by the solvent peak. Not all aliphatic signals in carbon spectrum were resolved. Characterisation was assisted by COSY, HSQC, and HMBC)

Di-N-heptanoyl tunicamycin (E2)

Heptanoic acid (5.5 μL, 0.039 mmol, 2.5 equiv) and DIC (6.1 μL, 0.039 mmol, 2.5 equiv) were added to DMF (0.25 mL) with the addition of TEA (2 μL) and DMAP (3.8 mg, 0.031 mmol, 2 equiv.) and stirred at room temperature for one hour. Then, α-D-glucosamine-(1″-11′)-tunicamyl uracil dihydrochloride Compound D (10 mg, 0.016 mmol) was dissolved in DMF (0.25 mL) with the addition of TEA (4.1 μL), and added to the octanoic acid reaction mixture. TEA was added to final of 4 equivalents (6.7 μL total). The reaction mixture was stirred at room temperature. The reaction progress was checked by TLC (1/3/6, H₂O/iPrOH/EtOAc) and HPLC. The reaction was stopped after 18 hrs. The product was purified by HPLC, eluted at 12 min. The lyophilised product was washed with DCM and MilliQ water and resulted in 4.8 mg of the final product, 39% yield. R_(f)=0.4 (1/3/6, H₂O/iPrOH/EtOAc); [α]_(D) ²⁰=+26.8±0.7 (c 0.2, MeOH); Mp N/A; ¹H NMR (500 MHz, MeOD) δ ppm 7.92 (d, J=8.1 Hz, 1H, H-6), 5.93 (d, J=6.0 Hz, 1H, H-1′), 5.75 (d, J=8.1 Hz, 1H, H-5), 4.94 (d, J=3.4 Hz, 1H, H-1″), 4.61 (d, J=8.5 Hz, 1H, H-11′), 4.24-4.16 (m, 2H, H-2′, H-3′), 4.06-3.99 (m, 2H, H-5′, H-5″), 3.95 (dd, J=10.2, 8.6 Hz, 1H, H-10′), 3.90 (dd, J=10.6, 3.5 Hz, 1H, H-2″), 3.87-3.81 (m, 2H, H-4′, H-6″), 3.77 (appt br d, J=9.1 Hz, 1H, H-7′), 3.71 3.62 (m, 4H, H-8′, H-9′, H-3″, H-6″), 3.34 (appt s, 1H, H-4″), 2.38 2.02 (m, 5H, 2×CH₂—^(fatty acyl), H-6′), 1.69-1.49 (m, 5H, 2×CH₂ ^(fatty acyl), H-6′), 1.41-1.28 (m, 15H, CH₂—^(fatty acyl)), 0.92 (t, J=6.8 Hz, 6H, CH₃ ^(fatty acyl)); ¹³C NMR (126 MHz, MeOD) δ ppm 177.18, 176.59, (2C, —N—C═O^(fatty acyl)), 166.17, (C-4), 152.64, (C-2), 142.77, (C-6), 103.06, (C-5), 101.28, (C-11′), 99.92, (C-1″), 89.77, (C-1′), 89.63, (C-4′), 75.53, (C-2′), 74.37, (C-5″), 73.04, (2C, C-8′, C-9′), 72.61, (C-4″), 72.49, (C-7′), 72.11, (C-3″), 70.89, (C-3′), 68.34, (C-5′), 63.27, (C-6″), 54.76, (C-2″), 54.47, (C-10′), 37.81, 37.22, (2C, —COCH₂—^(fatty acyl)), 35.94, (C-6′), 32.87, 32.81, 30.26, 27.01, 26.82, 23.68, (6C, —CH₂—^(fatty acyl)), 14.44. (1C, —CH₃ ^(fatty acyl)); IR (neat) ν: 3305 (O—H), 2927 (C—H), 2856 (C—H), 1682 (C═O), 1645 (C═O), 1552 (C═C), 1467 (CH₂), 1376 (CH₃), 1259 (C—O), 1094 (C—N); LRMS m/z (ESI⁺): 813 [(M+Na)⁺, 100%]; HRMS m/z (ESI⁺): calc. C₃₅H₅₈N₄O₁₆ (M+Na)⁺=813.3740, found 813.3708.

Di-N-octanoyl-tunicamycin (E3)

Octanoic acid (4.3 μL, 0.027 mmol, 2.5 equiv) and DIC (4.2 μL, 0.027 mmol, 2.5 equiv) were added to DMF (0.25 mL) with the addition of TEA (2 μL) and DMAP (2.7 mg, 0.022 mmol, 2 equiv.) and stirred at room temperature for one hour. Then, α-D-glucosamine-(1″-11′)-tunicamyl uracil dihydrochloride Compound D (7 mg, 0.011 mmol) was dissolved in DMF (0.25 mL) with the addition of TEA (4.1 μL), and added to the octanoic acid reaction mixture. TEA was added to final of 4 equivalents. The reaction mixture was stirred at room temperature. The reaction progress was checked by TLC (1/3/6, H₂O/iPrOH/EtOAc) and HPLC. The reaction was stopped after 7 days. The product was purified by HPLC, eluted at 13.5 min. The lyophilised product was washed with DCM and MilliQ water and resulted in 2.5 mg of the final product, 28% yield. R_(f)=0.3 (1/3/6, H₂O/iPrOH/EtOAc); [α]_(D) ²⁰=+57.4±0.4 (c 0.2, MeOH); Mp N/A; ¹H NMR (500 MHz, MeOD) δ ppm 7.91 (d, J=8.1 Hz, 1H, H-6), 5.92 (d, J=6.0 Hz, 1H, H-1′), 5.75 (d, J=8.1 Hz, 1H, H-5), 4.94 (d, J=3.4 Hz, 1H, H-1″), 4.60 (d, J=8.5 Hz, 1H, H-11′), 4.24 4.15 (m, 2H, H-2′, H-3′), 4.06 3.98 (m, 2H, H-5′, H-5″), 3.95 (dd, J=10.0, 8.6 Hz, 1H, H-10′), 3.90 (dd, J=10.6, 3.4 Hz, 1H, H-2″), 3.87 3.80 (m, 2H, H-4′, H-6″), 3.76 (dd, J=10.6, 1.6 Hz, 1H, H-7′), 3.70 3.61 (m, 4H, H-8′, H-9′, H-3″, H-6″), 3.34 (appt d, J=4.0 Hz, 1H, H-4″), 2.38 2.14 (m, 4H, 2×CH₂ ^(fatty acyl)), 2.10 (m, 1H, H-6′), 1.70-1.57 (m, 4H, 2×CH₂ ^(fatty acyl)), 1.53 (ddd, J=13.9, 11.4, 2.2 Hz, 1H, H-6′), 1.41-1.24 (appt br m, 16H, CH₂ ^(fatty acyl)), 0.91 (t, J=6.9 Hz, 6H, CH₃ ^(fatty acyl)); ¹³C NMR (126 MHz, MeOD) δ ppm 177.17, 176.58, (2C, —N—C═O^(fatty acyl)), 166.16 (C-4), 152.63 (C-2), 142.76 (C-6), 103.07 (C-5), 101.31 (C-11′), 99.95 (C-1″), 89.78 (C-1′), 89.63 (C-4′), 75.53 (C-2′), 74.37 (C-5″), 73.05 (2C, C-8′, C-9′), 72.61 (C-4″), 72.49 (C-7′), 72.11 (C-3″), 70.90 (C-3′), 68.34 (C-5′), 63.27 (C-6″), 54.76 (C-2″), 54.47 (C-10′), 37.81, 37.21 (2C, —COCH₂—^(fatty acyl)), 35.94 (C-6′), 33.00, 32.97, 30.56, 30.33, 30.27, 27.05, 26.85, 23.75 (8C, —CH₂—^(fatty acyl)), 14.45 (2C, —CH₃ ^(fatty acyl)); IR (neat) ν: 3297 (O—H), 2957 (C—H), 2925 (C—H), 2853 (C—H), 1684 (C═O), 1644 (C═O), 1556 (C═C), 1469 (CH₂), 1258 (C—O), 1091 (C—N), 1016 (═C—H); LRMS m/z (ESI⁻): 931 [(M+TFA−H)⁻, 100%]; HRMS m/z (ESI⁺): calc. C₃₇H₆₂N₄O₁₆Na (M+Na)⁺=841.4053, found 841.4045. (H-4″ signal in the 1H NMR spectrum observed to be partially overlapped by the solvent peak. Not all aliphatic signals in carbon spectrum were resolved. Characterisation was assisted by COSY and HSQC.)

Di-N-nonanoyl-tunicamycin (E4)

Nonanoic acid (6.8 μL, 0.039 mmol, 2.5 equiv) and DIC (6 μL, 0.039 mmol, 2.5 equiv) were added to DMF (0.25 mL) with the addition of TEA (2 μL) and DMAP (3.8 mg, 0.031 mmol, 2 equiv.) and stirred at room temperature for one hour. Then, α-D-glucosamine-(1″-11′)-tunicamyl uracil dihydrochloride Compound D (10 mg, 0.016 mmol) was dissolved in DMF (0.25 mL) with the addition of TEA (4.1 μL), and added to the octanoic acid reaction mixture. TEA was added to final of 4 equivalents (8.7 μL total). The reaction mixture was stirred at room temperature. The reaction progress was checked by TLC (1/3/6, H₂O/iPrOH/EtOAc) and HPLC. The reaction was stopped after 7 days. The product was purified by HPLC, eluted at 15 min. The lyophilised product was washed with DCM and MilliQ water and resulted in 3.4 mg of the final product, 26% yield. R_(f)=0.4 (1/3/6, H₂O/iPrOH/EtOAc); [α]_(D) ²⁰=+53.8±1.2 (c 0.3, MeOH); Mp N/A; ¹H NMR (500 MHz, MeOD) δ ppm 7.93 (d, J=8.1 Hz, 1H, H-6), 5.95 (d, J=5.9 Hz, 1H, H-1′), 5.77 (d, J=8.1 Hz, 1H, H-5), 4.96 (d, J=3.0 Hz, 1H, H-1″), 4.62 (d, J=8.6 Hz, 1H, H-11′), 4.26-4.18 (m, 2H, H-2′, H-3′), 4.08-4.00 (m, 2H, H-5′, H-5″), 3.97 (t, J=9.1 Hz, 1H, H-10′), 3.92 (dd, J=10.7, 3.2 Hz, 1H, H-2″), 3.89-3.81 (m, 2H, H-4′, H-6″), 3.78 (appt br d, J=9.8 Hz, 1H, H-7′), 3.73-3.63 (m, 4H, H-8′, H-9′, H-3″, H-6″), 3.36 (appt d, J=4.2 Hz, 1H, H-4″), 2.41-2.16 (m, 4H, 2×CH₂ ^(fatty acyl)), 2.12 (appt br t, J=12.1 Hz, 1H, H-6′), 1.71-1.59 (m, J=6.7 Hz, 4H, 2×CH₂ ^(fatty acyl)), 1.55 (appt br t, J=12.6 Hz, 1H, H-6′), 1.34 (s, 20H, CH₂ ^(fatty acyl)), 0.93 (t, J=6.5 Hz, 6H, CH₃ ^(fatty acyl)); ¹³C NMR (126 MHz, MeOD) δ ppm 177.17, 176.58 (2C, —N—C═O^(fatty acyl)), 166.16 (C-4), 152.63 (C-2), 142.76 (C-6), 103.06 (C-5), 101.32 (C-11′), 99.97 (C-1″), 89.78 (C-1′), 89.62 (C-4′), 75.53 (C-2′), 74.37 (C-5″), 73.06, 73.04 (2C, C-8′, C-9′), 72.60 (C-4″), 72.49 (C-7′), 72.11 (C-3″), 70.89 (C-3′), 68.33 (C-5′), 63.27 (C-6″), 54.76 (C-2″), 54.46 (C-10′), 37.82, 37.21 (2C, —COCH₂—^(fatty acyl)), 35.94 (C-6′), 33.10, 33.09, 30.62, 30.58, 30.45, 30.43, 27.05, 26.85, 23.77 (9C, —CH₂—^(fatty acyl)), 14.47 (1C, —CH₃ ^(fatty acyl)); IR (neat) ν: 3301 (O—H), 2923 (C—H), 2852 (CH), 1738 (C═O), 1646 (C═O), 1544 (C═C), 1420 (CH₂), 1366 (CH₃), 1229 (C—O), 1092 (CN), 1015 (═C—H); LRMS m/z (ESI⁻): 891 [(M+FA−H)⁻, 100%]; HRMS m/z (ESI⁻): calc. C₃₉H₆₅N₄O₁₆ (M−H)⁻=845.4401, found 845.4412. (H-4″ signal in the 1H NMR spectrum observed to be partially overlapped by the solvent peak. Not all aliphatic signals in carbon spectrum were resolved. Characterisation was assisted by COSY and HSQC)

Di-N-decanoyl-tunicamycin (E5)

Decanoic acid (4.7 mg, 0.027 mmol, 2.5 equiv) and DIC (4.2 μL, 0.027 mmol, 2.5 equiv) were added to DMF (0.25 mL) with the addition of TEA (2 μL) and DMAP (2.7 mg, 0.022 mmol, 2 equiv.) and stirred at room temperature for one hour. Then, α-D-glucosamine-(1″-11′)-tunicamyl uracil dihydrochloride Compound D (7 mg, 0.011 mmol) was dissolved in DMF (0.25 mL) with the addition of TEA (4.1 μL), and added to the decanoic acid reaction mixture. TEA was added to final of 4 equivalents. The reaction mixture was stirred at room temperature and reaction progress was checked by TLC (1/3/6, H₂O/iPrOH/EtOAc) and HPLC. The reaction was stopped after 63 hours. The product was purified by HPLC, eluted at 16.5 min. The lyophilised product was washed with DCM and MilliQ water and resulted in 3 mg of the final product, 31% yield. R_(f)=0.4 (1/3/6, H₂O/iPrOH/EtOAc); [α]_(D)=+38.0±0.6 (c 0.3, MeOH); Mp N/A; ¹H NMR (500 MHz, MeOD) δ ppm 7.91 (d, J=8.1 Hz, 1H, H-6), 5.92 (d, J=6.0 Hz, 1H, H-1′), 5.75 (d, J=8.1 Hz, 1H, H-5), 4.93 (d, J=3.4 Hz, 1H, H-1″), 4.59 (d, J=8.5 Hz, 1H, H-11′), 4.23-4.16 (m, 2H, H-2′, H-3′), 3.97-3.92 (m, 2H, H-5′, H-5″), 3.90 (appt t, J=8.5 Hz, 1H, H-10′), 3.84 (dd, J=10.6, 3.4 Hz, 1H, H-2″), 3.87-3.80 (m, 2H, H-4′, H-6″), 3.76 (appt br dd, J=10.7, 1.7 Hz, 1H, H-7′), 3.71-3.61 (m, 4H, H-8′, H-9′, H-3″, H-6″), 3.33 (appt d, J=5.8 Hz, 1H, H-4″), 2.38 2.02 (m, 4H, 2×CH₂ ^(fatty acyl)), 2.10 (m, 1H, H-6′), 1.69-1.49 (m, 4H, 2×CH₂ ^(fatty acyl)), 1.55 (m, 1H, H-6′), 1.30 (s, 24H, CH₂ ^(fatty acyl)), 0.90 (t, J=6.9 Hz, 6H, CH₃ ^(fatty acyl)); ¹³C NMR (126 MHz, MeOD) δ ppm 177.17, 176.58 (2C, —NC═O^(fatty acyl)), 166.16 (C-4), 152.63 (C-2), 142.76 (C-6), 103.06 (C-5), 101.33 (C-11′), 100.00 (C-1″), 89.78 (C-1′), 89.62 (C-4′), 75.53 (C-2′), 74.37 (C-5″), 73.07, 73.04 (2C, C-8′, C-9′), 72.60 (C-4″), 72.49 (C-7′), 72.11 (C-3″), 70.90 (C-3′), 68.33 (C-5′), 63.27 (C-6″), 54.76 (C-2″), 54.46 (C-10′), 37.82, 37.20 (2C, —COCH₂—^(fatty acyl)), 35.94 (C-6′), 33.12, 30.74, 30.72, 30.68, 30.63, 30.53, 27.05, 26.84, 23.78 (9C, —CH₂—^(fatty acyl)), 14.48 (2C, —CH₃ ^(fatty acyl)); IR (neat) ν: 3305 (O—H), 2922 (C—H), 2851 (C—H), 1683 (C═O), 1645 (C═O), 1551 (C═C), 1468 (CH₂), 1260 (C—O), 1094 (C—N), 1017 (═C—H); LRMS m/z (ESI⁻): 919 [(M+FA−H)⁻, 100%]; HRMS m/z (ESI⁺): calc. C₄₁H₇₀N₄O₁₆Na (M+Na)⁺=897.4679, found 897.4666. (H-4″ signal in the 1H NMR spectrum observed to be partially overlapped by the solvent peak. Not all aliphatic signals in carbon spectrum were resolved. Characterisation was assisted by COSY and HSQC.)

Di-N-undecanoyl-tunicamycin (E6)

Undecanoic acid (5 mg, 0.027 mmol, 2.5 equiv) and DIC (4.2 μL, 0.027 mmol, 2.5 equiv) were added to DMF (0.25 mL) with the addition of TEA (2 μL) and DMAP (2.7 mg, 0.022 mmol, 2 equiv.) and stirred at room temperature for one hour. Then, α-D-glucosamine-(1″-11′)-tunicamyl uracil dihydrochloride Compound D (7 mg, 0.011 mmol) was dissolved in DMF (0.25 mL) with the addition of TEA (4.1 μL), and added to the undecanoic acid reaction mixture. TEA was added to final of 4 equivalents. The reaction mixture was stirred at room temperature and reaction progress was checked by TLC (1/3/6, H₂O/iPrOH/EtOAc) and HPLC. The reaction was stopped after 68 hours. The product was purified by HPLC, eluted at 18 min. The lyophilised product was washed with DCM and MilliQ water and resulted in 3 mg of the final product, 30% yield. R_(f)=0.4 (1/3/6, H₂O/iPrOH/EtOAc); [α]_(D) ²⁰=+30.9±0.4 (c 0.25, MeOH); Mp N/A; ¹H NMR (500 MHz, MeOD) δ ppm 7.91 (d, J=8.1 Hz, 1H, H-6), 5.92 (d, J=6.0 Hz, 1H, H-1′), 5.75 (d, J=8.1 Hz, 1H, H-5), 4.93 (d, J=3.4 Hz, 1H, H-1″), 4.60 (d, J=8.5 Hz, 1H, H-11′), 4.23 4.15 (m, 2H, H-2′, H-3′), 4.05-3.98 (m, 2H, H-5′, H-5″), 3.95 (m, 1H, H-10′), 3.90 (dd, J=10.6, 3.4 Hz, 1H, H-2″), 3.86-3.80 (m, 2H, H-4′, H-6″), 3.76 (appt br dd, J=10.7, 1.8 Hz, 1H, H-7′), 3.71-3.61 (m, 4H, H-8′, H-9′, H-3″, H-6″), 3.34 (m, 1H, H-4″), 2.37-2.14 (m, 4H, 2×CH₂ ^(fatty acyl)), 2.13-2.05 (m, 1H, H-6′), 1.68-1.56 (m, 4H, 2×CH₂ ^(fatty acyl)), 1.57-1.49 (m, 1H, H-6′), 1.30 (appt br s, 32H, CH₂ ^(fatty acyl)), 0.90 (t, J=6.9 Hz, 6H, CH₃ ^(fatty acyl)); ¹³C NMR (126 MHz, MeOD) δ ppm 177.17, 176.57, (2C, —N—C═O^(fatty acyl)), 166.22 (C-4), 152.67 (C-2), 142.76 (C-6), 103.06 (C-5), 101.34 (C-11′), 100.02 (C-1″), 89.78 (C-1′), 89.62 (C-4′), 75.53 (C-2′), 74.37 (C-5″), 73.07, 73.05 (2C, C-8′, C-9′), 72.59 (C-4″), 72.49 (C-7′), 72.10 (C-3″), 70.90 (C-3′), 68.33 (C-5′), 63.27 (C-6″), 54.76 (C-2″), 54.46 (C-10′), 37.82, 37.20 (2C, —COCH₂—^(fatty acyl)), 35.94 (C-6′), 33.13, 30.82, 30.79, 30.77, 30.68, 30.64, 30.63, 30.54, 27.05, 26.83, 23.79 (11C, —CH₂ ^(fatty acyl)), 14.48 (2C, —CH₃ ^(fatty acyl)); IR (neat) ν: 3297 (O—H), 2956 (C—H), 2921 (C—H), 2852 (C—H), 1738 (C═O), 1719 (C═O), 1680 (C═C), 1645 (C═O), 1550 (N—H), 1468 (CH₂), 1366 (CH₃), 1229 (C—O—C), 1217 (C—OH), 1260 (C—O), 1092 (C—N), 1017 (═C—H); LRMS m/z (ESI⁻): 947 [(M+FA−H)⁻, 100%]; HRMS m/z (ESI⁺): calc. C₄₃H₇₃N₄O₁₆ (M−H)⁻=901.5027, found 901.5015. (H-4″ signal in the ¹H NMR spectrum observed to be partially overlapped by the MeOD solvent peak. Not all aliphatic signals in carbon spectrum were resolved. Characterisation was assisted by COSY and HSQC.)

Di-N-dodecanoyl-tunicamycin (E7)

Dodecanoic acid (5.4 mg, 0.027 mmol, 2.5 equiv) and DIC (4.2 μL, 0.027 mmol, 2.5 equiv) were added to DMF (0.25 mL) with the addition of TEA (2 μL) and DMAP (2.7 mg, 0.022 mmol, 2 equiv.) and stirred at room temperature for one hour. Then, α-D-glucosamine-(1″-11′)-tunicamyl uracil dihydrochloride Compound D (7 mg, 0.011 mmol) was dissolved in DMF (0.25 mL) with the addition of TEA (4.1 μL), and added to the dodecanoic acid reaction mixture. TEA was added to final of 4 equivalents. The reaction mixture was stirred at room temperature and reaction progress was checked by TLC (1/3/6, H₂O/iPrOH/EtOAc) and HPLC. The reaction was stopped after 68 hours. The product was purified by HPLC, eluted at 20.5 min. The lyophilised product was washed with DCM and MilliQ water and resulted in 3 mg of the final product, 29% yield. R_(f)=0.4 (1/3/6, H₂O/iPrOH/EtOAc); [α]_(D) ²⁰=+15.9±0.4 (c 0.25, MeOH); Mp N/A; ¹H NMR (500 MHz, MeOD) δ 7.92 (d, J=8.1 Hz, 1H, H-6), 5.93 (d, J=5.9 Hz, 1H, H-1′), 5.76 (d, J=8.1 Hz, 1H, H-5), 4.94 (d, J=3.5 Hz, 1H, H-1″), 4.60 (d, J=8.5 Hz, 1H, H-11′), 4.24-4.17 (m, 2H, H-2′, H-3′), 4.08-3.99 (m, 2H, H-5′, H-5″), 3.96 (m, J=8.6 Hz, 1H, H-10′), 3.91 (dd, J=10.6, 3.4 Hz, 1H, H-2″), 3.88-3.80 (m, 2H, H-4′, H-6″), 3.77 (appt br dd, J=11.1, 1.8 Hz, 1H, H-7′), 3.72-3.61 (m, 4H, H-8′, H-9′, H-3″, H-6″), 2.39-2.15 (m, 4H, 2×CH₂ ^(fatty acyl)), 2.11 (m, 1H, H-6′), 1.70-1.57 (m, 4H, 2×CH₂ ^(fatty acyl)), 1.54 (m, 1H, H-6′), 1.40-1.28 (appt broad m, 32H, CH₂ ^(fatty acyl)), 0.91 (t, J=6.9 Hz, 6H, CH3 fatty acyl); ¹³C NMR (126 MHz, MeOD) δ ppm 177.17, 176.57 (2C, —N—C═O^(fatty acyl)), 166.16 (C-4), 152.63 (C-2), 142.76 (C-6), 103.06 (C-5), 101.35 (C-11′), 100.04 (C-1″), 89.77 (C-1′), 89.62 (C-4′), 75.52 (C-2′), 74.37 (C-5″), 73.08, 73.04 (2C, C-8′, C-9′), 72.60 (C-4″), 72.49 (C-7′), 72.10 (C-3″), 70.90 (C-3′), 68.33 (C-5′), 63.27 (C-6″), 54.76 (C-2″), 54.45 (C-10′), 37.82, 37.19 (2C, —COCH₂—^(fatty acyl)), 35.94 (C-6′), 30.87, 30.83, 30.79, 30.77, 30.68, 30.65, 30.63, 30.55, 27.05, 26.83, 23.79 (11C, —CH₂—^(fatty acyl)), 14.48 (2C, —CH₃ ^(fatty acyl)); IR (neat) ν: 3297 (O—H), 2956 (C—H), 2921 (C—H), 2851 (C—H), 1682 (C═O), 1646 (C═O), 1556 (C═C), 1468 (CH₂), 1260 (C—O), 1092 (C—N), 1016 (═C—H); LRMS m/z (ESI⁻): 976 [(M+FA−H)⁻, 100%]; HRMS m/z (ESI⁺): calc. C₄₅H₇₈N₄O₁₆Na (M+Na)⁺=953.5305, found 953.5334. (H-4″ signal in the 1H NMR spectrum observed to be partially overlapped by the solvent peak. Not all aliphatic signals in carbon spectrum were resolved. Characterisation was assisted by COSY and HSQC)

General Procedure

The general procedure given below was used for the synthesis of compounds of formula E (as shown in the schemes at the beginning of this Example, Example 1).

A 0.022 M solution of NaOMe in MeOH was prepared by dissolving sodium (4.1 mg, 0.177 mmol) in anhydrous MeOH (8 mL). The resulting NaOMe solution was then added to Tri-N-(tert-butoxylcarbonyl)-octa-O-acetyl-tunicamycin 5 (260 mg, 0.177 mmol) in a 25 mL round-bottomed flask and the resulting orange solution stirred for 4 h under argon. The reaction mixture was diluted with MeOH (5 mL) and carefully quenched with DOWEX 50 W×8 ft form resin. The resin was removed by filtration and the filtrate concentrated in vacuo. The resulting yellow solid was washed with Et₂O (2×2 mL) to remove hydrolyzed lipids and dried under an argon stream. The resulting light-yellow solid was dissolved in TFA (4 mL) and stirred at ambient temperature for 1 h. The reaction mixture was then concentrated in vacuo and azeotroped with toluene (2×4 mL). The resulting solid was washed with Et₂O (5 mL) and dried under an argon stream to yield crude diamine as an off-white solid. In a separate flask, the carboxylic acid (0.372 mmol) and HATU (141 mg, 0.372 mmol) were dissolved in dry DMF (2 mL) and cooled to 0° C. DIPEA (123 uL, 0.708 mmol) was added and the resulting yellow solution stirred at 0° C. for 15 min. A solution of the crude diamine in DMF (2 mL) was added and the resulting yellow solution stirred at ambient temperature for 16 22 h. The reaction mixture was concentrated in vacuo and redissolved in 1:1:1 MeCN:H₂O:^(i)PrOH (6 mL) and purified by RP-HPLC: Column=Phenomenex Synergi 4u Fusion hydro-RP 80a; flow rate=12 mL/min; detection=254 nm; solvent A=0.1% formic acid in H₂O and solvent B=0.1% formic acid in MeCN; gradient=30% B (2 min), 30-80% B (10 min), 80-98% B (1 min), 98% B (5 min), 98-30% B (1 min), 30% B (5 min). Product containing fractions were pooled, concentrated, frozen and lyophilized to yield the compounds E. Compounds E3 and E4 were prepared by this method in respective yields of 22% and 19% over three steps.

Preparation of Biocompatible Formulation for In Vivo Testing

To prepare a biocompatible formulation for in vivo testing, Compounds E3 and E4 can be dissolved in concentrations >10 mg/mL in an aqueous solution of Tween 80 (0.5%) and sodium hydroxide (0.1-0.5%).

Example 2: Bioactivity of Lipid Altered Tunicamycin Analogues and Underlying Scaffolds Against Bacillus subtilis (EC1524) and Bacillus cereus (ATCC11778)

Underlying scaffolds A, B, C and D and lipid-altered analogues E1 to E7 were assayed for potency against Bacillus subtilis (EC1524) and Bacillus cereus (ATCC11778). Naturally extracted tunicamycin (TM) was also assayed as a control.

Bioactivity was assessed using the Kirby-Bauer disc diffusion susceptibility test. Oxoid Blank Discs were impregnated with the desired test substance. A 0.5 McFarland standard inoculum was prepared by adding 3-5 single colonies to 10 mL MH broth in a 15 mL falcon tube and standardised to 0.5 McFarland standard. The inoculum was used within 10 minutes. A sterile cotton swab was dipped in the inoculum, gently pressed against the side of the tube to remove excess liquid, and generously streaked on MH agar plate to fully cover the plate. The impregnated disc was carefully placed on the agar. The plate was incubated at 35° C. for 20 hrs overnight. A digital calliper was used to measure the zone diameter. The recorded zone diameter is an average of three zone diameters measured of one zone.

Each 6 mm disc was impregnated with 5 μg of the relevant compound (TM, A, B, C, D, or any of E1 to E7), and the diffusion zone recorded after 20 hours.

FIG. 1 shows results of the Kirby-Bauer disc diffusion susceptibility test conducted using Bacillus subtilis as a test organism. FIG. 1 and Table 1 below shows result obtained for E2 to E7 and TM. Non-lipidated scaffolds A, B, C and D were completely inactive against Bacillus subtilis. FIG. 1 and Table 1 also shows analogous results obtained using Bacillus cereus as a test organism. Results are shown for E2 to E7 and TM. The activities of the tested substances against Bacillus subtilis and Bacillus cereus are shown in Table 1. Values quoted are zone diameters, with larger numbers indicating higher antibacterial activity. Non-lipidated scaffolds A, B, C and D were completely inactive against Bacillus cereus. With both organisms Bacillus cereus and Bacillus subtilis, the most active lipid altered tunicamycin analogues displayed essentially identical antibacterial activity to natural tunicamycin (TM).

TABLE 1 Reference in Diffusion distance (mm) Substance FIG. 1 Bacillus subtilis Bacillus cereus TM TM 15 13 E2 3 10 E3 4 16 12 E4 5 16 13 E5 6 10 9 E6 7 6 7 E7 8

Minimal and half maximal inhibitory concentrations (MIC and IC50 values) and minimal bactericidal concentration (MBC) of TM and the lipid modified tunicamycin analogues E1 to E7 were assayed against Bacillus subtilis and Bacillus cereus.

In a sterile 96-well plate, serial dilutions were made with the test substance to final volume of 50 μL. Inoculum was then prepared in Mueller-Hinton broth to 0.5 McFarland and diluted before adding 50 μL to the well to make 1×10⁵ CFU/mL. The culture plate was incubated at 35° C. for 20-24 hours. A positive growth control and sterility wells were also prepared along with the culture wells. Absorbance at OD₆₀₀ was taken using BMG Labtech SPECTROstar Omega spectrophotometer. MIC was determined by the lowest concentration without growth. IC50 was determined from plotting a dose-response curve. Data were analysed using Graph Pad PRISM 5.01 software. Dose-response curves were plotted from three independent data sets with SEM error bars. To determine the MBC, using a multi-channel pipette, 1 μL of culture broth was taken from the same 96-well microdilution growth plate and carefully inoculated on surface of MH agar plate. The plate is then incubated for additional 20 hours at 35° C. The MBC value is the lowest concentration without observed growth on the agar. Results are shown in Table 2.

TABLE 2 Bacillus subtilis Bacillus cereus Sub- MIC MBC IC50 MIC MBC IC50 stance (μg/mL) (μg/mL) (μg/mL) (μg/mL) (μg/mL) (μg/mL) TM 0.0015  >0.0015  0.001484  0.195    25  0.003163 E1 6.25 >100  0.415 100 >200  6.292 E2 6.25  >50  3.39 100 >200 13.33 E3 0.78  >0.98  0.20114  6.25    50  0.7823 E4 0.024  >0.06  0.01457  0.78    25  0.07229 E5 0.39  >0.39  0.1141  0.39    12.5  0.0461 E6 1.56  >6.25  0.8519  0.78    25  0.08781 E7 100 >200 58.87  50 >200  1.402

Example 3: Bioactivity of Lipid Altered Tunicamycin Analogues and Underlying Scaffolds Against Pseudomonas aeruginosa (ATCC27853)

Underlying scaffolds A, B, C and D and lipid-varied analogues E1 to E7 were assayed for potency against Pseudomonas aeruginosa (ATCC27853), according to the methods of Example 2. Results of the Kirby-Bauer disc diffusion susceptibility test conducted using Pseudomonas aeruginosa (ATCC27853) as a test organism are shown in FIG. 2 and in Table 3. MIC, MBC and IC50 values were also obtained as in Example 2. Results are shown in Table 3.

TABLE 3 Pseudomonas aeruginosa Reference in Diffusion distance MIC MBC IC50 Substance FIG. 2 (mm) (μg/mL) (μg/mL) (μg/mL) TM TM >400 >400 >400 E1 200 >400 70.29 E2 3 7 100 >400 62.44 E3 4 9 100 >400 46.54 E4 5 13 100 400 54.98 E5 6 12 100 400 53.46 E6 7 12 100 400 63.17 E7 8 8 200 >400 81.94

Inhibitory activity against Pseudomonas aeruginosa was observed for E4 to E6. Surprisingly, this inhibitory activity was greater than that observed for natural tunicamycin.

Example 4: Bioactivity of Lipid Altered Tunicamycin Analogues and Underlying Scaffolds Against Mycobacterium tuberculosis H37RV

One of the most pernicious Gram-positive pathogens is Mycobacterium tuberculosis. It is responsible for 1.3 million deaths per annum and it is estimated that a third of the world's population is infected. It is also resistant to common antibacterial treatments.

TM and the lipid-varied analogues E1 to E7 were assayed for potency against Mycobacterium tuberculosis H37RV. MIC values were determined as in Example 2, except that MIC values were determined in GAST/Fe growth medium and in 7H9/ADC/Tw (ADC=Albumin dextrose complex; Tw=Tween) growth medium, and were assessed at 1 and 2 weeks. Results are shown in Table 4.

TABLE 4 1-week MIC (μg/mL) 2-week MIC (μg/mL) Substance 7H9/ADC/Tw GAST/Fe 7H9/ADC/Tw GAST/Fe Water No inhibition No inhibition No inhibition No inhibition Methanol No inhibition No inhibition No inhibition No inhibition TM 0.7 0.12 0.9 0.18 E1 22.5 5.6 22.5 11.2 E2 7.5 2.8 7.5 2.8 E3 0.94 0.23 1.4 0.35 E4 0.23 0.029 0.35 0.04 E5 1.4 0.18 1.4 0.35 E6 5.6 2.8 5.6 2.8 E7 22.5 11.2 30 11.2

Surprisingly, the MIC values for lipid-altered tunicamycin analogue E4 are significantly lower, in some cases approximately 5-fold lower than naturally occurring tunicamycin TM. This signifies that the lipid-altered tunicamycin analogue E4 is more potent than TM. Furthermore, these values are comparable with current first line drugs such as Isoniazid (for which MIC=0.1 in 7H9 growth medium) and Rifampicin (MIC=0.125-0.25 in 7H9 growth medium).

Example 5: Determination of Cytotoxicity of Lipid Altered Tunicamycin Analogues and Underlying Scaffolds in Human Liver Cells and in Human Kidney Cells

Underlying scaffolds A, B, C and D and lipid-varied analogues E1 to E7 were assayed for cytotoxicity towards human liver cells (Hep2G) and human kidney cells (HEK293). Following administration of the relevant compound (A, B, C, D, or any of E1 to E7), cells were examined both by analysis of the resulting proliferation dose response curve and by analysis of any morphological changes by microscopy.

HepG2 and HEK293 Cell Culture.

Mammalian cells were cultured in DMEM medium supplemented with 10% heat inactivated fetal bovine serum (FBS, v/v). The cultures were maintained in a humidified incubator at 37° C. in 5% CO₂/95% air. FBS was reduced to 2% for the cell proliferation assay.

Cell Proliferation Assay

In sterile 96-well plate, each well was seeded with 1×10⁵ cells. The cells were then grown confluent overnight in 100 μL DMEM with 10% FBS. The medium was replenished with DMEM with 2% FBS and added vehicle control or test substance the next day. For test substance in methanol, stock was added to 25 μL of DMEM with 2% FBS or PBS and placed in a laminar flow hood to let the methanol evaporate (about 1-3 hrs). Once the methanol has evaporated, DMEM with 2% FBS was added to final volume of 100 μL of desired test concentration. A blank methanol control was also made to ensure any cytotoxicity does not result from methanol contamination. Cells were grown for additional 24 hrs. The cell viability was determined by using a Promega CellTiter 96 AQueous One Solution Cell Proliferation Assay System following the manufacturer's protocol.

Incubation of the cells with TM over a period of 24 hours showed both clear cytotoxicity (FIG. 3) and morphological changes (FIG. 4). A dose response curve for TM is shown in FIG. 3. Specifically, half lethal dose values (LD₅₀) for TM were 42.55±4.45 μg/mL towards HepG2 liver cells and 71.92±24.84 μg/mL towards HEK293 kidney cells. Over longer time periods, cell stress responses were observed that also distorted proliferation assays.

In contrast to the results obtained with TM, the scaffolds (A to D) and the lipidated variants E1 to E7 displayed no significant toxicity towards HepG2 liver cells or HEK293 kidney cells. No dose response curve is shown for A to D or E1 to E7 due to the low cytotoxicity of these compounds. Surprisingly, at doses as high as 400 μg/mL, minimal cytotoxicity was observed. Higher concentrations resulted in precipitation of tunicamycin and lipid variants E1 to E7. Even more surprisingly, incubation of HepG2 liver cells and HEK293 kidney cells for 24 hours with 400 μg/mL E1 to E7 led to a high level (>75%) of viable cells exhibiting no morphological changes.

Minimum lethal dosages for TM and E1 to E7 are therefore as shown in Table 5.

TABLE 5 Minimum lethal dose/μg/mL Substance HepG2 HEK293 TM 100 100 E1 >400 >400 E2 >400 >400 E3 >400 >400 E4 >400 >400 E5 >400 >400 E6 >400 >400 E7 >400 >400

Example 6: Determination of the Relative Therapeutic Index of Lipid Altered Tunicamycin Analogues Using Bacillus subtilis (EC1524), Bacillus cereus (ATCC11778), and Mycobacterium tuberculosis H3 7RV

The Relative Therapeutic Index (RTI) was determined. RTI is the ratio between the minimal lethal dose calculated in Example 5 and the minimal inhibition concentration (determined in Examples 2 to 4). The microdilution broth test and cytotoxicity test were carried out by serial 2-fold dilutions. In cases when no cytotoxicity was detectable at 400 μg/mL, a minimal lethal dose of 800 μg/mL was used to calculate the RTI. Results are shown in Table 6.

TABLE 6 RTI M. tuberculosis M. tuberculosis (2 weeks in (2 weeks in Substance B. subtilis B. cereus 7H9/ADC/Tw) GAST/Fe) TM 66667 513 111 556 D 8 8 13 13 E1 128 8 36 71 E2 128 8 107 286 E3 1026 128 571 2286 E4 33333 1026 2286 20000 E5 2051 2051 571 2286 E6 513 1026 143 286 E7 8 16 27 71

Example 7: Pharmacokinetic/Pharmacodynamics (PK/PD) Studies on Intraperitoneal (IP) Injections

After extensive solubility testing a suitable formulation was found for the tunicamycin analogues. The formulation includes 90% phosphate-buffer-saline (PBS) at pH=7.3, 10% ethanol, with 1% Tween-80 surfactant added to the final mixture. This formulation is suitable for solubility of up to 1.5 mg/mL of the compounds.

A single-dose PK study was done using 16 mice at a dose of 30 mg/kg for the TM-8 analogue, di-N-octanoyl-tunicamycin. This gave the PK curve shown in FIG. 5. The compound was easily detectable 6 hours after the injection, with some detectability. This study confirmed that the formulation was suitable for injections, and the drug is stable enough in physiological conditions. 

1. An oligosaccharide which is a compound according to Formula (I), or a pharmaceutically acceptable salt thereof,

wherein: [Base] is a natural nucleobase selected from adenine, cytosine, guanine, thymine and uracil; each R¹, which may be the same or different, is independently H, OH, —OPO(OH)₂, or halogen; each R², which may be the same or different, is independently H, halogen, or C₁ to C₂ alkyl; R³ and R⁴, which may be the same or different, are each independently H, OH, halogen, C₁ to C₂ alkyl, C₁ to C₂ alkoxy, or —NR¹⁰R¹¹; each R⁵, which may be the same or different, is independently H, halogen, or C₁ to C₂ alkyl; each R⁶, which may be the same or different, is independently OH, halogen, —OPO(OH)₂, —OCO₂CH₃, —NHCOCH₃ or C₁ to C₂ alkoxy; one or more R⁷ and/or one or more R⁸ is a group —NHC(O)R⁹; the remaining groups R⁷, which may be the same or different, are independently H, halogen, or C₁ to C₂ alkyl; and the remaining groups R⁸, which may be the same or different, are independently OH, halogen, —OPO(OH)₂, —OCO₂CH₃, —NHCOCH₃ or C₁ to C₂ alkoxy; each R⁹, which may be the same or different, is independently C₃ to C₂₀ alkyl, C₃ to C₂₀ alkenyl, or C₃ to C₂₀ alkynyl, wherein R⁹ may be unsubstituted or may be substituted by from 1 to 6 substituents selected from halogen, OH, C₁ to C₄ alkoxy and —NR¹⁰R¹¹; and each R¹⁰ and R¹¹, which may be the same or different, is independently H or C₁ to C₄ alkyl.
 2. An oligosaccharide according to claim 1 which is a compound according to Formula (II), or a pharmaceutically acceptable salt thereof

wherein R¹ to R¹¹ and [Base] are as defined in claim
 1. 3. An oligosaccharide according to claim 1 or 2 wherein [Base] is thymine or uracil.
 4. An oligosaccharide according to any one of the preceding claims wherein each R¹, which may be the same or different, is independently OH or —OPO(OH)₂.
 5. An oligosaccharide according to any one of the preceding claims wherein each R², which may be the same or different, is independently H or methyl.
 6. An oligosaccharide according to any one of the preceding claims wherein R³ and R⁴ are each H.
 7. An oligosaccharide according to any one of the preceding claims wherein each R⁵, which may be the same or different, is independently H or C₁ to C₂ alkyl.
 8. An oligosaccharide according to any one of the preceding claims wherein each R⁶, which may be the same or different, is independently OH, —NHCOCH₃ or —OPO(OH)₂.
 9. An oligosaccharide according to any one of the preceding claims wherein one of the R⁷ and/or R⁸ groups which are —NHC(O)R⁹ is bonded to the C2″ carbon.
 10. An oligosaccharide according to any one of the preceding claims wherein the total number of R⁷ and R⁸ groups which are —NHC(O)R⁹ is from 1 to 3; the remaining groups R⁷, which may be the same or different, are independently H or C₁ to C₂ alkyl, and the remaining groups R⁸, which may be the same or different, are independently OH, —NHCOCH₃ or —OPO(OH)₂.
 11. An oligosaccharide according to claim 10 wherein one group R⁸ is —NHC(O)R⁹; the groups R⁷, which may be the same or different, are independently H or C₁ to C₂ alkyl; and the remaining groups R⁸, which may be the same or different, are independently OH, —NHCOCH₃ or —OPO(OH)₂, according to Formula (IV)


12. An oligosaccharide according to any one of the preceding claims wherein each R⁹, which may be the same or different, is independently C₄ to C₁₆ alkyl, or C₄ to C₁₆ alkenyl, wherein R⁹ is unsubstituted or substituted by from 1 to 4 substituents selected from halogen, OH, C₁ to C₄ alkoxy, and —NR¹⁰R¹¹.
 13. An oligosaccharide according to any one of the preceding claims wherein each R⁹, which may be the same or different, is independently C₆ to C₁₂ alkyl, or C₆ to C₁₂ alkenyl, wherein R⁹ is unsubstituted or substituted by from 1 to 3 substituents selected from halogen, OH and C₁ to C₄ alkoxy.
 14. An oligosaccharide according to any one of the preceding claims wherein each R⁹, which may be the same or different, is independently an unsubstituted C₇ to C₉ alkyl group.
 15. An oligosaccharide according to any one of the preceding claims having a structure according to Formula (III)

wherein each R⁹, which may be the same or different, is defined as in any one of claims 1 or 12 to
 14. 16. An oligosaccharide according to claim 15 wherein R⁹ is selected from


17. A pharmaceutical composition comprising an oligosaccharide according to any of claims 1 to 16 and a pharmaceutically acceptable carrier or diluent.
 18. An oligosaccharide according to any of claims 1 to 16 or a pharmaceutical composition according to claim 17 for use in treating or preventing bacterial infection.
 19. The oligosaccharide or pharmaceutical composition for use according to claim 18, wherein the infection is caused by one or more gram-positive bacterium.
 20. The oligosaccharide or pharmaceutical composition for use according to claim 18, wherein the infection is caused by one or more gram-negative bacterium.
 21. The oligosaccharide or pharmaceutical composition for use according to claim 18, wherein the bacterial infection is caused by Bacillus, Pseudomonas, Mycobacterium, Staphylococcus, or Escherichia.
 22. The oligosaccharide or pharmaceutical composition for use according to claim 21, wherein the bacterial infection is caused by Mycobacterium tuberculosis.
 23. The oligosaccharide or pharmaceutical composition for use according to claim 18, wherein the oligosaccharide or pharmaceutical composition is for use in treating or preventing tuberculosis. 